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    Chemistry

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    Also known as: 554-13-2, Dilithium carbonate, Lithonate, Lithobid, Lithane, Carbonic acid, dilithium salt
    Molecular Formula
    CLi2O3
    Molecular Weight
    73.9  g/mol
    InChI Key
    XGZVUEUWXADBQD-UHFFFAOYSA-L
    FDA UNII
    2BMD2GNA4V
    Lithium Carbonate
    A lithium salt, classified as a mood-stabilizing agent. Lithium ion alters the metabolism of BIOGENIC MONOAMINES in the CENTRAL NERVOUS SYSTEM, and affects multiple neurotransmission systems.
    1 2D Structure

    Lithium Carbonate

    2 Identification
    2.1 Computed Descriptors
    2.1.1 IUPAC Name
    dilithium;carbonate
    2.1.2 InChI
    InChI=1S/CH2O3.2Li/c2-1(3)4;;/h(H2,2,3,4);;/q;2*+1/p-2
    2.1.3 InChI Key
    XGZVUEUWXADBQD-UHFFFAOYSA-L
    2.1.4 Canonical SMILES
    [Li+].[Li+].C(=O)([O-])[O-]
    2.2 Other Identifiers
    2.2.1 UNII
    2BMD2GNA4V
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. Bicarbonate, Lithium

    2. Carbonate, Dilithium

    3. Carbonate, Lithium

    4. Cp 15,467 61

    5. Cp-15,467-61

    6. Cp15,46761

    7. Dilithium Carbonate

    8. Eskalith

    9. Lithane

    10. Lithium Bicarbonate

    11. Lithobid

    12. Lithonate

    13. Lithotabs

    14. Micalith

    15. Nsc 16895

    16. Nsc-16895

    17. Nsc16895

    18. Priadel

    19. Quilinorm Retard

    20. Quilinorm-retard

    21. Quilinormretard

    2.3.2 Depositor-Supplied Synonyms

    1. 554-13-2

    2. Dilithium Carbonate

    3. Lithonate

    4. Lithobid

    5. Lithane

    6. Carbonic Acid, Dilithium Salt

    7. Eskalith

    8. Lithotabs

    9. Carbonic Acid Lithium Salt

    10. Liskonum

    11. Lithizine

    12. Micalith

    13. Priadel

    14. Limas

    15. Eskalith Cr

    16. Camcolit

    17. Carbolitium

    18. Neurolepsin

    19. Lithium Carbonicum

    20. Nsc-16895

    21. Candamide

    22. Carbolith

    23. Eutimin

    24. Hypnorex

    25. Lithicarb

    26. Lithinate

    27. Lithionate

    28. Liticar

    29. Manialith

    30. Maniprex

    31. Litard

    32. Lithea

    33. Plenur

    34. Quilonum Retard

    35. Pfi-lithium

    36. Lithium Phasal

    37. Pfl-lithium

    38. Litho-carb

    39. Cp-15467-61

    40. Lithium Carbonate (li2co3)

    41. Cp-15,467-61

    42. Mfcd00011084

    43. 2bmd2gna4v

    44. Chebi:6504

    45. Carbonic Acid Lithium Salt (li2co3)

    46. Lithium Carbonate (2:1)

    47. Cp 15467-61

    48. Ceglution

    49. Phasal

    50. Cp-1546761

    51. Teralithe [french]

    52. Lithium Carbonate Nanoparticles

    53. Carbolithium

    54. Teralithe

    55. Lithium, Reference Standard Solution

    56. Dilithium;carbonate

    57. Li2 (c O3)

    58. Carbonic Acid Dilithium Salt

    59. Ccris 3153

    60. Hsdb 3351

    61. Einecs 209-062-5

    62. Unii-2bmd2gna4v

    63. Carbolithium Ifi

    64. Lithium Qd

    65. Eskalith (tn)

    66. Lithobid (tn)

    67. Lithium Carbonate [usan:usp:jan]

    68. Starbld0023766

    69. Lithium Carbonate Powder

    70. Li2co3

    71. Dilithium Trioxidocarbonate

    72. Ec 209-062-5

    73. Lithium Carbonate [mi]

    74. Lithium Carbonate [jan]

    75. Chembl1200826

    76. Dtxsid1023784

    77. Lithium Carbonate (jp17/usp)

    78. Lithium Carbonate [hsdb]

    79. Lithium Carbonate [inci]

    80. Lithium Carbonate [usan]

    81. Lithium Carbonate [vandf]

    82. Lithium Carbonicum [hpus]

    83. Lithium Carbonate [mart.]

    84. Lithium Carbonate [usp-rs]

    85. Lithium Carbonate [who-dd]

    86. Lithium Carbonate [who-ip]

    87. Str02638

    88. Carbonic Acid, Lithium Salt (1:2)

    89. Dilithium Carbonate [who-ip]

    90. Lithium Carbonate, Acs Reagent Grade

    91. Akos015904647

    92. Angc-554-13-2

    93. Db14509

    94. Lithii Carbonas [who-ip Latin]

    95. Lithium Carbonate [orange Book]

    96. Lithium Carbonate [ep Monograph]

    97. Lithium Carbonate [usp Monograph]

    98. B7705

    99. Ft-0627895

    100. L0224

    101. C07964

    102. D00801

    103. Dilithium Carbonate, Dilithium Salt, Carbonic Acid

    104. Q410174

    2.4 Create Date
    2004-09-16
    3 Chemical and Physical Properties
    Molecular Weight 73.9 g/mol
    Molecular Formula CLi2O3
    Hydrogen Bond Donor Count0
    Hydrogen Bond Acceptor Count3
    Rotatable Bond Count0
    Exact Mass74.01675073 g/mol
    Monoisotopic Mass74.01675073 g/mol
    Topological Polar Surface Area63.2 Ų
    Heavy Atom Count6
    Formal Charge0
    Complexity18.8
    Isotope Atom Count0
    Defined Atom Stereocenter Count0
    Undefined Atom Stereocenter Count0
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count3
    4 Drug and Medication Information
    4.1 Drug Information
    1 of 4  
    Drug NameLithium carbonate
    Drug LabelEach capsule for oral administration contains 150 mg, 300 mg or 600 mg of Lithium Carbonate USP.Inactive IngredientsThe capsules contain talc. The hard gelatin shell consists of gelatin, titanium dioxide, sodium lauryl sulphate and FD & C Red 40.The..
    Active IngredientLithium carbonate
    Dosage FormTablet, extended release; Tablet; Capsule
    RouteOral
    Strength150mg; 600mg; 300mg; 450mg
    Market StatusPrescription
    CompanyMylan Pharms; Alembic; Hetero Labs Ltd Iii; Sun Pharm Inds; Hikma Pharms; Roxane; Glenmark Generics

    2 of 4  
    Drug NameLithobid
    Drug LabelLITHOBID tablets contain lithium carbonate, a white odorless alkaline powder with molecular formula Li2CO3 and molecular weight 73.89. Lithium is an element of the alkali-metal group with atomic number 3, atomic weight 6.94, and an emission line at...
    Active IngredientLithium carbonate
    Dosage FormTablet, extended release
    RouteOral
    Strength300mg
    Market StatusPrescription
    CompanyAni Pharms

    3 of 4  
    Drug NameLithium carbonate
    Drug LabelEach capsule for oral administration contains 150 mg, 300 mg or 600 mg of Lithium Carbonate USP.Inactive IngredientsThe capsules contain talc. The hard gelatin shell consists of gelatin, titanium dioxide, sodium lauryl sulphate and FD & C Red 40.The..
    Active IngredientLithium carbonate
    Dosage FormTablet, extended release; Tablet; Capsule
    RouteOral
    Strength150mg; 600mg; 300mg; 450mg
    Market StatusPrescription
    CompanyMylan Pharms; Alembic; Hetero Labs Ltd Iii; Sun Pharm Inds; Hikma Pharms; Roxane; Glenmark Generics

    4 of 4  
    Drug NameLithobid
    Drug LabelLITHOBID tablets contain lithium carbonate, a white odorless alkaline powder with molecular formula Li2CO3 and molecular weight 73.89. Lithium is an element of the alkali-metal group with atomic number 3, atomic weight 6.94, and an emission line at...
    Active IngredientLithium carbonate
    Dosage FormTablet, extended release
    RouteOral
    Strength300mg
    Market StatusPrescription
    CompanyAni Pharms

    4.2 Therapeutic Uses

    Antidepressive Agents; Antimanic Agents; Antithyroid Agents; Enzyme Inhibitors

    National Library of Medicine's Medical Subject Headings online file (MeSH, 1999)

    Most prepn currently used in the U.S. are tablets or capsules of lithium carbonate. Slow-release prepn of lithium carbonate also are available, as is a liq prepn of lithium citrate (with 8 mEq of Li+, equivalent to 300 mg of carbonate salt, per 5 mL or 1 teaspoonful of citrate liq). Salts other than the carbonate have been used, but the carbonate salt is favored for tablets and capsules because it is relatively less hygroscopic and less irritating to the gut than other salts, especially the chloride salt. /Li therapy/

    Hardman, J.G., L.E. Limbird, P.B., A.G. Gilman. Goodman and Gilman's The Pharmacological Basis of Therapeutics. 10th ed. New York, NY: McGraw-Hill, 2001., p. 511

    Lithium /carbonate and citrate/ is indicated as the primary agent in the treatment of acute manic and hypomanic episodes in bipolar disorder, and for maintenance therapy to help diminish the intensity and frequency of subsequent manic episodes in patients with a history of mania. /Included in US product labeling/

    Thomson/Micromedex. Drug Information for the Health Care Professional. Volume 1, Greenwood Village, CO. 2007., p. 1844

    Lithium /carbonate and citrate/ is used in some patients as the agent of choice in the prevention of bipolar depression. Clinicians have observed a diminished intensity and frequency of severe depressive episodes. /Included in US product labeling/

    Thomson/Micromedex. Drug Information for the Health Care Professional. Volume 1, Greenwood Village, CO. 2007., p. 1844

    For more Therapeutic Uses (Complete) data for LITHIUM CARBONATE (28 total), please visit the HSDB record page.

    4.3 Drug Warning

    Because of potential effects of lithium upon thyroid and renal function, appropriate indices of these functions should be measured prior to start of treatment, then monitored periodically as therapy proceeds.

    Miller, R. R., and D. J. Greenblatt. Handbook of Drug Therapy. New York: Elsevier North Holland, 1979., p. 580

    Lithium carbonate should not be used in patients with cardiovascular or renal disease. ...Should not be used in children under 12 yr of age.

    Osol, A. and J.E. Hoover, et al. (eds.). Remington's Pharmaceutical Sciences. 15th ed. Easton, Pennsylvania: Mack Publishing Co., 1975., p. 1025

    Outpatients and their families should be warned that the patient must discontinue lithium therapy immediately and consult a physician if signs of lithium intoxication such as muscle twitching, tremor, mild ataxia, drowsiness, muscle weakness, diarrhea, or vomiting occur. Patients also should be warned that lithium may impair their ability to perform activities requiring mental alertness or physical coordination (e.g., operating machinery, driving a motor vehicle).

    McEvoy, G.K. (ed.). American Hospital Formulary Service. AHFS Drug Information. American Society of Health-System Pharmacists, Bethesda, MD. 2007., p. 2570

    Lithium should be used cautiously in patients with preexisting cardiovascular or thyroid disease. Patients with underlying cardiovascular disease should be observed carefully for signs and symptoms of arrhythmia (including periodic ECG determinations), and serum lithium concentrations should be kept within the therapeutic range since nodal arrhythmias may occur. Patients with underlying hypothyroidism should have thyroid function (T3, T4, and TSH concentrations) evaluated yearly and be given supplemental thyroid therapy when needed.

    McEvoy, G.K. (ed.). American Hospital Formulary Service. AHFS Drug Information. American Society of Health-System Pharmacists, Bethesda, MD. 2007., p. 2571

    For more Drug Warnings (Complete) data for LITHIUM CARBONATE (45 total), please visit the HSDB record page.

    4.4 Drug Indication

    Lithium is used as a mood stabilizer, and is indicated for the treatment of manic episodes and maintenance of bipolar disorder.

    FDA Label

    5 Pharmacology and Biochemistry
    5.1 Pharmacology

    Lithium's mechanism of action is still unknown. Lithium's therapeutic action may be due to a number of effects, ranging from inhibition of enzymes such as glycogen synthase kinase 3, inositol phosphatases, or modulation of glutamate receptors.

    5.2 MeSH Pharmacological Classification

    Antidepressive Agents

    Mood-stimulating drugs used primarily in the treatment of affective disorders and related conditions. Several MONOAMINE OXIDASE INHIBITORS are useful as antidepressants apparently as a long-term consequence of their modulation of catecholamine levels. The tricyclic compounds useful as antidepressive agents (ANTIDEPRESSIVE AGENTS, TRICYCLIC) also appear to act through brain catecholamine systems. A third group (ANTIDEPRESSIVE AGENTS, SECOND-GENERATION) is a diverse group of drugs including some that act specifically on serotonergic systems. (See all compounds classified as Antidepressive Agents.)

    Enzyme Inhibitors

    Compounds or agents that combine with an enzyme in such a manner as to prevent the normal substrate-enzyme combination and the catalytic reaction. (See all compounds classified as Enzyme Inhibitors.)

    Antimanic Agents

    Agents that are used to treat bipolar disorders or mania associated with other affective disorders. (See all compounds classified as Antimanic Agents.)

    5.3 FDA Pharmacological Classification
    5.3.1 Pharmacological Classes
    Mood Stabilizer [EPC]
    5.4 Absorption, Distribution and Excretion

    Absorption

    Lithium absorption is rapid and oral bioavailability is close to 100%.

    Route of Elimination

    Lithium is primarily eliminated through the kidneys and elimination in the feces is insignificant.

    Volume of Distribution

    Apparent volume of distribution is 0.7 to 1.0L/kg.

    Clearance

    Clearance is generally between 10 and 40mL/min but may be as low as 15mL/min in elderly patients and those with renal impairment.

    ... Lithium /carbonate/ crosses placenta and is present in mother and fetus in same concentration.

    American Medical Association, Council on Drugs. AMA Drug Evaluations Annual 1994. Chicago, IL: American Medical Association, 1994., p. 313

    Lithium /carbonate/ is completely absorbed six to eight hours after oral administration. Since the onset of action is slow (five to ten days), parenteral administration is of no advantage. The plasma half-life is 17 to 36 hours, and this drug is eliminated almost entirely by the kidneys. Lithium clearance averages approximately 20% of creatinine clearance, but significant variability exists among patients.

    American Medical Association, Council on Drugs. AMA Drug Evaluations Annual 1994. Chicago, IL: American Medical Association, 1994., p. 313

    The population pharmacokinetics of lithium were determined using the nonlinear mixed effects model (NONMEM) program in 79 psychiatric inpatients who were at least 18 yr old, had normal renal function, and were receiving lithium carbonate 2 or 3 times daily. With the initial model, the mean lithium volume of distribution was 32.8 L and the mean lithium clearance was 1.36 L/hr. With an intermediate model, lithium clearance estimates improved on the basis of patient size (weight and body surface area), daily lithium dosage, age, gender, and race. When only the most significant variables, lean body weight and creatinine clearance, were retained, a final model was obtained that yielded a coefficient of variation for lithium clearance of about 24% and gave fairly accurate predictions of steady-state lithium concentrations (coefficient of variation, about 16%). It was concluded that analysis of lithium pharmacokinetics with the nonlinear mixed-effects model program suggested that lean body weight and creatinine clearance are important predictors of lithium clearance.

    PMID:2049899 Jermain DE et al; Clin Pharm 10 (May): 376-381 (1991)

    Lithium disposition in plasma, red blood cells and urine was studied in acute self-poisoned patient upon chronic lithium therapy (n=4) and in chronic intoxicated patients receiving oral lithium (n=10). Following acute intoxication upon chronic lithium therapy, lithium pharmacokinetics did not differ from previous reports. Terminal plasma half life ranged from 19.0-29.0 hr and RBC/plasma ratio was 0.32 +/- 0.11. the distribution volume of the terminal phase, Vz, was estimated at 0.84 +/- 0.32 L/kg and renal clearance was 0.38 +/- 0.11 ml/mn/kg. After chronic intoxication lithium pharmacokinetics differed from those of the acute patients. Terminal plasma half-life ranged from 36.5-79.4 hr and zero-order decline appeared in 8 of the 10 patients. The RBC/plasma ratio was 0.87 +/- 0.22 on admission. Vz was estimated at 0.71 +/- 0.27 L/kg and renal clearance was 0.16 +/- 0.07 ml/mn/kg. These modifications in lithium elimination kinetics could be related to the decrease in the glomerular filtration rate with age or renal dysfunction in this group of patients.

    PMID:7582387 Ferron G et al; Int J Clin Pharmacol Ther 33 (6): 351-5 (1995)

    For more Absorption, Distribution and Excretion (Complete) data for LITHIUM CARBONATE (22 total), please visit the HSDB record page.

    5.5 Metabolism/Metabolites

    Lithium carbonate is not metabolized before excretion.

    5.6 Biological Half-Life

    The half life of lithium carbonate is 18 to 36 hours. Other sources say it may be 7 to 20 hours.

    The plasma half-life is 17 to 36 hours.

    American Medical Association, Council on Drugs. AMA Drug Evaluations Annual 1994. Chicago, IL: American Medical Association, 1994., p. 313

    The plasma half-life (in healthy volunteers) shows a considerable variability: from 5 to 40 hr, with most values between 15 and 30 hr, it depends on the duration of treatment as well as on kidney function and age. /Li+/

    Chang, L.W. (ed.). Toxicology of Metals. Boca Raton, FL: Lewis Publishers, 1996, p. 455

    The usual elimination half-life is 12 to 27 hr, but it may rise to nearly 60 hr if renal excretion is compromised. /Li+/

    Klaassen, C.D. (ed). Casarett and Doull's Toxicology. The Basic Science of Poisons. 6th ed. New York, NY: McGraw-Hill, 2001., p. 852

    ... The elimination half-life averages 20 to 24 hr. /Li+/

    Hardman, J.G., L.E. Limbird, P.B., A.G. Gilman. Goodman and Gilman's The Pharmacological Basis of Therapeutics. 10th ed. New York, NY: McGraw-Hill, 2001., p. 508

    For more Biological Half-Life (Complete) data for LITHIUM CARBONATE (9 total), please visit the HSDB record page.

    5.7 Mechanism of Action

    Lithium's mechanism of action is still unknown. However, the inositol depletion theory suggests 3 main potential targets. These targets are inositol monophosphatase, inositol polyphosphatase, and glycogen synthase kinase 3(GSK-3). The Inositol depletion theory suggests lithium behaves as an uncompetitive inhibitor of inositol monophosphatase in a manner inversely proportional to the degree of stimulus. This inhibition lowers levels of inositol triphosphate. However, stronger inhibitors of inositol monophosphatase are not as clinically effective and low levels of inositol triphosphate are associated with memory impairment. Lithium acts on inositol polyphosphatase as an uncompetitive inhibitor. This inhibition is thought to have multiple downstream effects that have yet to be clarified. Lithium regulates phosphorylation of GSK-3 which regulates other enzymes through phosphorylation. Lithium can also inhibit GSK-3 through interfering with the magnesium ion in the active site.

    Although its antimanic mechanism of action has not been fully determined, lithium is known to affect a variety of neurohumoral signal transduction mechanisms. ... Lithium /lithium carbonate/ counteracts mood changes and is considered the most specific antimanic drug for the prophylaxis and treatment of bipolar disorder.

    American Medical Association, Council on Drugs. AMA Drug Evaluations Annual 1994. Chicago, IL: American Medical Association, 1994., p. 311

    In animal brain tissue, Li+ at concn of 1 to 10 mEq/L inhibits the depolarization-provoked and Ca+2-dependent release of norepinephrine and dopamine, but not serotonin, from nerve terminals. Li+ may even enhance the release of serotonin, especially in the limbic system, at least transiently. The ion has little effect on catecholamine-sensitive adenylyl cyclase activity or on the binding of ligands to monoamine receptors in brain tissue, although there is some evidence that Li+ can inhibit the effects of receptor-blocking agents that cause supersensitivity in such systems. Li+ can modify some hormonal responses mediated by adenylyl cyclase or phospholipase C in other tissues, including the actions of antidiuretic and thyroid-stimulating hormones on the actions of antidiuretic and thyroid-stimulating hormones on their peripheral target tissues. In part, the actions of Li+ may reflect its ability to interfere with the activity of both stimulatory and inhibitory GTP-binding proteins (Gs and Gi) by keeping them in their less active alpha-beta-gamma trimer state. /Li+/

    Hardman, J.G., L.E. Limbird, P.B., A.G. Gilman. Goodman and Gilman's The Pharmacological Basis of Therapeutics. 10th ed. New York, NY: McGraw-Hill, 2001., p. 508

    Lithium inhibits the phosphatase that liberates inositol (I) from inositol phosphate (IP) ... Li+ ... can modify the abundance or function of G proteins and effectors, as well as protein kinases and several cell and nuclear regulatory factors. /Li+, from figure/

    Hardman, J.G., L.E. Limbird, P.B., A.G. Gilman. Goodman and Gilman's The Pharmacological Basis of Therapeutics. 10th ed. New York, NY: McGraw-Hill, 2001., p. 494

    Mechanistically, the Li effect results from its substitution for body cations, eg, sodium and potassium, resulting in multisystemic actions. A partial substitution for normal cations causes changes in ion exchange and transfer in cellular processes. Incorporation of Li into membrane structures may alter responses to hormones and the coupling of energy processes ... Among the factors that may modify Li toxicity and kinetics are the type of the poisoning, the presence of the underlying disease, and renal impairment. /Li+/

    Chang, L.W. (ed.). Toxicology of Metals. Boca Raton, FL: Lewis Publishers, 1996, p. 455

    For more Mechanism of Action (Complete) data for LITHIUM CARBONATE (22 total), please visit the HSDB record page.

    API Reference Price

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ESTILL, S,C 29 918 USA SDNF UNITED STATES","customerAddress":"28\/A, IDA,"},{"dataSource":"API Import","activeIngredients":"","year":"2025","qtr":"Q1","strtotime":1737311400,"product":"LITHIUM DIFLUOROPHOSPHATE LITHIUM DIFLUOROPHOSPHATE","address":"Survey No. 16\/3, 26 & 27,","city":"Panch Mahals,","supplier":"ANHUI MEISENBAO TECHNOLOGY CO LTD","supplierCountry":"CHINA","foreign_port":"HONG KONG","customer":"GFCL EV PRODUCTS LIMITED","customerCountry":"INDIA","quantity":"1.00","actualQuantity":"1","unit":"KGS","unitRateFc":"490.5","totalValueFC":"495.5","currency":"USD","unitRateINR":"42722.5","date":"20-Jan-2025","totalValueINR":"42722.46","totalValueInUsd":"495.5","indian_port":"Bombay Air","hs_no":"29319090","bill_no":"7891599","productDescription":"API","marketType":"REGULATED MARKET","country":"CHINA","selfForZScoreResived":"Pharma Grade","supplierPort":"HONG KONG","supplierAddress":"No.20, Wutong Middle Road, Economic Development Zone, Longhu Industria l Park Huaibei, , China","customerAddress":"Survey No. 16\/3, 26 & 27,"},{"dataSource":"API Import","activeIngredients":"","year":"2025","qtr":"Q1","strtotime":1739298600,"product":"225770-CONF LITHIUM BIS(TRIMETHYLSILYL)AMIDE, 1.0M S (FOR LA B PURPOSE) (0.850 L)","address":"PLOT.NO.12,BOMMASANDRA-JIGANI LINK","city":"BANGALORE","supplier":"N\/A","supplierCountry":"UNITED STATES","foreign_port":"CHICAGO","customer":"SIGMA ALDRICH CHEMICALS PRIVATE LIMITED","customerCountry":"INDIA","quantity":"1.00","actualQuantity":"1","unit":"KGS","unitRateFc":"91.7","totalValueFC":"93.2","currency":"INR","unitRateINR":"8106","date":"12-Feb-2025","totalValueINR":"8106","totalValueInUsd":"93.2","indian_port":"Bangalore Air","hs_no":"29319090","bill_no":"8304110","productDescription":"API","marketType":"REGULATED MARKET","country":"UNITED STATES","selfForZScoreResived":"Pharma Grade","supplierPort":"CHICAGO","supplierAddress":"N\/A","customerAddress":"PLOT.NO.12,BOMMASANDRA-JIGANI LINK"},{"dataSource":"API Import","activeIngredients":"","year":"2025","qtr":"Q1","strtotime":1740162600,"product":"A17921.0B LITHIUM ACETATE DIHYDRATE, 99% A17921.0B LITHIUM ACETATE DIHYDRATE, 99%","address":"403-404, B WING, DELPHI,,HIRANANDA","city":"MUMBAI,MAHARASHTRA","supplier":"ALFA AESAR","supplierCountry":"UNITED KINGDOM","foreign_port":"MANCHESTER","customer":"THERMO FISHER SCIENTIFIC","customerCountry":"INDIA","quantity":"1.00","actualQuantity":"1","unit":"KGS","unitRateFc":"94.8","totalValueFC":"95.7","currency":"GBP","unitRateINR":"8319.6","date":"22-Feb-2025","totalValueINR":"8319.59","totalValueInUsd":"95.7","indian_port":"Hyderabad Air","hs_no":"29152990","bill_no":"8516650","productDescription":"API","marketType":"REGULATED MARKET","country":"UNITED KINGDOM","selfForZScoreResived":"Pharma Grade","supplierPort":"MANCHESTER","supplierAddress":"AVOCADO RESEARCH CHEMICALS LTD SHOR E ROAD, PORT OF HEYSHAM, INDUSTRIAL PARK, HEYSHAM, LANCASTER LA3 2XY,E United Kingdom","customerAddress":"403-404, B WING, DELPHI,,HIRANANDA"},{"dataSource":"API Import","activeIngredients":"","year":"2025","qtr":"Q1","strtotime":1741285800,"product":"L-SELECTRIDE IN THF SOLUTION (CALSELECT LI 1M IN THF-[LITHIUM TRI-SEC-BUTYLBOROHYDRIDE IN TETRAHYDROFURAN 1M]CHEMICAL","address":"Floor No.22, Plot No.1, Survey No.83\/1, Galaxy Tower","city":"Hyderabad","supplier":"ASCENSUS SPECIALTIES","supplierCountry":"UNITED STATES","foreign_port":"LONG BEACH","customer":"APITORIA PHARMA PRIVATE LIMITED","customerCountry":"INDIA","quantity":"3354.00","actualQuantity":"3354","unit":"KGS","unitRateFc":"67","totalValueFC":"227785.6","currency":"USD","unitRateINR":"5882.6","date":"07-Mar-2025","totalValueINR":"19730240.4","totalValueInUsd":"227785.6","indian_port":"Madras Sea","hs_no":"29319090","bill_no":"8748425","productDescription":"API","marketType":"REGULATED MARKET","country":"UNITED STATES","selfForZScoreResived":"Pharma Grade","supplierPort":"LONG BEACH","supplierAddress":"1424 MARS EVANS CITY ROAD EVANS CI TY PA 16033 , , UNITED STATES SDNF UNITED STATES","customerAddress":"Floor No.22, Plot No.1, Survey No.83\/1, Galaxy Tower"}]
    19-Jan-2021
    27-Mar-2025
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    DOSAGE - CAPSULE;ORAL - 150MG

    USFDA APPLICATION NUMBER - 17812

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    DOSAGE - CAPSULE;ORAL - 300MG

    USFDA APPLICATION NUMBER - 17812

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    DOSAGE - CAPSULE;ORAL - 600MG

    USFDA APPLICATION NUMBER - 17812

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    DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 300M...DOSAGE - TABLET, EXTENDED RELEASE;ORAL - 300MG

    USFDA APPLICATION NUMBER - 18027

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    DOSAGE - TABLET;ORAL - 300MG

    USFDA APPLICATION NUMBER - 18558

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    ABOUT THIS PAGE

    Looking for 554-13-2 / Lithium Carbonate API manufacturers, exporters & distributors?

    Lithium Carbonate manufacturers, exporters & distributors 1

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    PharmaCompass offers a list of Lithium Carbonate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Lithium Carbonate manufacturer or Lithium Carbonate supplier for your needs.

    Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Lithium Carbonate manufacturer or Lithium Carbonate supplier.

    PharmaCompass also assists you with knowing the Lithium Carbonate API Price utilized in the formulation of products. Lithium Carbonate API Price is not always fixed or binding as the Lithium Carbonate Price is obtained through a variety of data sources. The Lithium Carbonate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.

    API | Excipient name

    Lithium Carbonate

    Synonyms

    554-13-2, Dilithium carbonate, Lithonate, Lithobid, Lithane, Carbonic acid, dilithium salt

    Cas Number

    554-13-2

    Unique Ingredient Identifier (UNII)

    2BMD2GNA4V

    About Lithium Carbonate

    A lithium salt, classified as a mood-stabilizing agent. Lithium ion alters the metabolism of BIOGENIC MONOAMINES in the CENTRAL NERVOUS SYSTEM, and affects multiple neurotransmission systems.

    Camcolit Manufacturers

    A Camcolit manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Camcolit, including repackagers and relabelers. The FDA regulates Camcolit manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Camcolit API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

    click here to find a list of Camcolit manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

    Camcolit Suppliers

    A Camcolit supplier is an individual or a company that provides Camcolit active pharmaceutical ingredient (API) or Camcolit finished formulations upon request. The Camcolit suppliers may include Camcolit API manufacturers, exporters, distributors and traders.

    click here to find a list of Camcolit suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

    Camcolit USDMF

    A Camcolit DMF (Drug Master File) is a document detailing the whole manufacturing process of Camcolit active pharmaceutical ingredient (API) in detail. Different forms of Camcolit DMFs exist exist since differing nations have different regulations, such as Camcolit USDMF, ASMF (EDMF), JDMF, CDMF, etc.

    A Camcolit DMF submitted to regulatory agencies in the US is known as a USDMF. Camcolit USDMF includes data on Camcolit's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Camcolit USDMF is kept confidential to protect the manufacturer’s intellectual property.

    click here to find a list of Camcolit suppliers with USDMF on PharmaCompass.

    Camcolit JDMF

    The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.

    The Camcolit Drug Master File in Japan (Camcolit JDMF) empowers Camcolit API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).

    PMDA reviews the Camcolit JDMF during the approval evaluation for pharmaceutical products. At the time of Camcolit JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.

    click here to find a list of Camcolit suppliers with JDMF on PharmaCompass.

    Camcolit KDMF

    In Korea, the Ministry of Food and Drug Safety (MFDS) is in charge of regulating pharmaceutical products and services.

    Pharmaceutical companies submit a Camcolit Drug Master File in Korea (Camcolit KDMF) to the MFDS, which includes comprehensive information about the production, processing, facilities, materials, packaging, and testing of Camcolit. The MFDS reviews the Camcolit KDMF as part of the drug registration process and uses the information provided in the Camcolit KDMF to evaluate the safety and efficacy of the drug.

    After submitting a Camcolit KDMF to the MFDS, the registered manufacturer can provide importers or distributors with the registration number without revealing confidential information to Korean business partners. Applicants seeking to register their Camcolit API can apply through the Korea Drug Master File (KDMF).

    click here to find a list of Camcolit suppliers with KDMF on PharmaCompass.

    Camcolit CEP

    A Camcolit CEP of the European Pharmacopoeia monograph is often referred to as a Camcolit Certificate of Suitability (COS). The purpose of a Camcolit CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Camcolit EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Camcolit to their clients by showing that a Camcolit CEP has been issued for it. The manufacturer submits a Camcolit CEP (COS) as part of the market authorization procedure, and it takes on the role of a Camcolit CEP holder for the record. Additionally, the data presented in the Camcolit CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Camcolit DMF.

    A Camcolit CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Camcolit CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.

    click here to find a list of Camcolit suppliers with CEP (COS) on PharmaCompass.

    Camcolit WC

    A Camcolit written confirmation (Camcolit WC) is an official document issued by a regulatory agency to a Camcolit manufacturer, verifying that the manufacturing facility of a Camcolit active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Camcolit APIs or Camcolit finished pharmaceutical products to another nation, regulatory agencies frequently require a Camcolit WC (written confirmation) as part of the regulatory process.

    click here to find a list of Camcolit suppliers with Written Confirmation (WC) on PharmaCompass.

    Camcolit NDC

    National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Camcolit as an active pharmaceutical ingredient (API).

    Finished drug products

    The FDA updates the NDC directory daily. The NDC numbers for Camcolit API and other APIs are published in this directory by the FDA.

    Unfinished drugs

    The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

    Pharmaceutical companies that manufacture Camcolit as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

    Compounded drug products

    The NDC directory also contains data on finished compounded human drug products that contain Camcolit and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Camcolit NDC to their finished compounded human drug products, they may choose to do so.

    click here to find a list of Camcolit suppliers with NDC on PharmaCompass.

    Camcolit GMP

    Camcolit Active pharmaceutical ingredient (API) is produced in GMP-certified manufacturing facility.

    GMP stands for Good Manufacturing Practices, which is a system used in the pharmaceutical industry to make sure that goods are regularly produced and monitored in accordance with quality standards. The FDA’s current Good Manufacturing Practices requirements are referred to as cGMP or current GMP which indicates that the company follows the most recent GMP specifications. The World Health Organization (WHO) has its own set of GMP guidelines, called the WHO GMP. Different countries can also set their own guidelines for GMP like China (Chinese GMP) or the EU (EU GMP).

    PharmaCompass offers a list of Camcolit GMP manufacturers, exporters & distributors, which can be sorted by USDMF, JDMF, KDMF, CEP (COS), WC, API price, and more, enabling you to easily find the right Camcolit GMP manufacturer or Camcolit GMP API supplier for your needs.

    Camcolit CoA

    A Camcolit CoA (Certificate of Analysis) is a formal document that attests to Camcolit's compliance with Camcolit specifications and serves as a tool for batch-level quality control.

    Camcolit CoA mostly includes findings from lab analyses of a specific batch. For each Camcolit CoA document that a company creates, the USFDA specifies specific requirements, such as supplier information, material identification, transportation data, evidence of conformity and signature data.

    Camcolit may be tested according to a variety of international standards, such as European Pharmacopoeia (Camcolit EP), Camcolit JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Camcolit USP).

    Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
    For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.
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