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ACTIVE PHARMA INGREDIENTS

43 API Suppliers, 28 USDMF, 14 CEP/COS, 13 EU WC, 16 NDC API, 21 Listed Suppliers, $ API Reference Price

43 API Suppliers
28 USDMF
14 CEP/COS
13 EU WC
16 NDC API
21 Listed Suppliers
$ API Reference Price

INTERMEDIATES

6 Intermediates Suppliers

6 Intermediates Suppliers

FINISHED DOSAGE FORMULATIONS

215 FDF Dossiers, 95 FDA Orange Book, 40 Europe, 55 Canada, 8 South Africa, 17 Listed Dossiers

215 FDF Dossiers
95 FDA Orange Book
40 Europe
55 Canada
8 South Africa
17 Listed Dossiers

DRUG PRODUCT COMPOSITIONS

TABLET;ORAL - EQ 10MG BASE, TABLET;ORAL - EQ 20MG BASE, TABLET;ORAL - EQ 40MG BASE

drugProductComposition
TABLET;ORAL - EQ 10MG BASE
TABLET;ORAL - EQ 20MG BASE
TABLET;ORAL - EQ 40MG BASE

RELATED EXCIPIENT COMPANIES

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relatedExcipients
2 Rochem International Inc
17 SPI Pharma
2 Seqens
8 DKSH
7 Faran Shimi Pharmaceutical
11 Boai NKY Pharmaceuticals Ltd
14 Gangwal Healthcare
6 Nanjing Well Pharmaceutical
1 Pfanstiehl
4 ACG Worldwide
7 Actylis
1 Aeon Procare
2 Alcedo Pharmachem
9 Anhui Sunhere Pharmaceutical Excipients Co.,Ltd
1 Avesta Pharma
33 BASF
2 Clariant
10 Corel Pharma Chem
6 DFE Pharma
2 Finar
12 Gangwal Chemicals
1 Huzhou Sunflower Pharmaceutical
7 Ideal Cures Pvt Ltd
5 Ingredion Pharma Solutions
33 Kerry
3 Kima Chemical
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15 Microlex e.U
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8 Pluviaendo
4 Prachin Chemical
1 Qianhao Chemical (Hebei) Co., Ltd
2 Qualicaps
29 Roquette
13 Seppic
7 Shanghai Shenmei Pharmaceutical Technology Co., Ltd
1 Shanghai Welltone Material Technology Co., Ltd
2 Shijiazhuang Huaxu Pharmaceutical
12 Sigachi Industries
2 The Dow Chemical Company
2 Ulanqab Kema New Material
1 Valens Pharmachem
4 Vasa Pharmachem
1 Zhejiang Huakang Pharmaceutical

EXCIPIENTS BY APPLICATIONS

100 Fillers, Diluents & Binders, 56 Coating Systems & Additives, 49 Direct Compression, 41 Disintegrants & Superdisintegrants, 33 Controlled & Modified Release, 31 Granulation, 31 Solubilizers, 31 Thickeners and Stabilizers, 27 Film Formers & Plasticizers, 24 Parenteral, 21 Taste Masking, 21 Co-Processed Excipients, 19 Topical, 18 Chewable & Orodispersible Aids, 18 Lubricants & Glidants, 9 Emulsifying Agents, 9 Empty Capsules, 8 API Stability Enhancers, 5 Coloring Agents, 5 Rheology Modifiers, 5 Surfactant & Foaming Agents, 4 Vegetarian Capsules, 1 Soft Gelatin

DIGITAL CONTENT

1 DATA COMPILATION #PharmaFlow, 2 NEWS #PharmaBuzz

media
1 DATA COMPILATION #PharmaFlow
2 NEWS #PharmaBuzz

GLOBAL SALES INFORMATION

2 US Medicaid Prescriptions, 15 Finished Drug Prices

globalSalesInformation
2 US Medicaid Prescriptions
15 Finished Drug Prices

MARKET PLACE

2 APIs

marketPlace
2 APIs

PATENTS & EXCLUSIVITIES

6 Health Canada Patents

patents
6 Health Canada Patents

REF. STANDARDS & IMPURITIES

3 EDQM , 1 USP , 1 Others

otherSolutions
3 EDQM
1 USP
1 Others

Synopsis

ACTIVE PHARMA INGREDIENTS

API Suppliers

USDMF

CEP/COS

JDMF

EU WC

KDMF

NDC API

VMF

Listed Suppliers

API REF. PRICE (USD/KG)

$ 168

MARKET PLACE

API

FDF

6INTERMEDIATES

FINISHED DOSAGE FORMULATIONS

215

FDF Dossiers

FDA Orange Book

Europe

Canada

Australia

South Africa

Listed Dossiers

0 DRUGS IN DEVELOPMENT

DRUG PRODUCT COMPOSITIONS

REF. STANDARDS OR IMPURITIES

EDQM

USP

Others

PATENTS & EXCLUSIVITIES

US Patents

US Exclusivities

Health Canada Patents

DIGITAL CONTENT

Data Compilation #PharmaFlow

Stock Recap #PipelineProspector

Weekly News Recap #Phispers

News #PharmaBuzz

GLOBAL SALES INFORMATION

US Medicaid (USD)

62,057,930

Annual Reports (USD Million)

Finished Drug Prices

328 RELATED EXCIPIENT COMPANIES

566EXCIPIENTS BY APPLICATIONS

Chemistry

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Also known as: 59729-32-7, Citalopram hbr, Celexa, Cipramil, 1-(3-(dimethylamino)propyl)-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile hydrobromide, Elopram

Molecular Formula

C₂₀H₂₂BrFN₂O

Molecular Weight

405.3 g/mol

InChI Key

WIHMBLDNRMIGDW-UHFFFAOYSA-N

FDA UNII

I1E9D14F36

A furancarbonitrile that is one of the SELECTIVE SEROTONIN REUPTAKE INHIBITORS used as an antidepressant. The drug is also effective in reducing ethanol uptake in alcoholics and is used in depressed patients who also suffer from TARDIVE DYSKINESIA in preference to tricyclic antidepressants, which aggravate dyskinesia.

1 2D Structure

Citalopram Hydrobromide

2 Identification

2.1 Computed Descriptors

2.1.1 IUPAC Name

1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-3H-2-benzofuran-5-carbonitrile;hydrobromide

2.1.2 InChI

InChI=1S/C20H21FN2O.BrH/c1-23(2)11-3-10-20(17-5-7-18(21)8-6-17)19-9-4-15(13-22)12-16(19)14-24-20;/h4-9,12H,3,10-11,14H2,1-2H3;1H

2.1.3 InChI Key

WIHMBLDNRMIGDW-UHFFFAOYSA-N

2.1.4 Canonical SMILES

CN(C)CCCC1(C2=C(CO1)C=C(C=C2)C#N)C3=CC=C(C=C3)F.Br

2.2 Other Identifiers

2.2.1 UNII

I1E9D14F36

2.3 Synonyms

2.3.1 MeSH Synonyms

1. Celexa

2. Citalopram

3. Cytalopram

4. Lu-10-171

5. Lu10171

6. Seropram

2.3.2 Depositor-Supplied Synonyms

1. 59729-32-7

2. Citalopram Hbr

3. Celexa

4. Cipramil

5. 1-(3-(dimethylamino)propyl)-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile Hydrobromide

6. Elopram

7. Seropram

8. Bonitrile Hbr

9. Nitalapram Hbr

10. Lu 10-171-b

11. Citalopram (hydrobromide)

12. Citalopram, Hydrobromide Salt

13. Lu 10-171 Hbr

14. 1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-3h-2-benzofuran-5-carbonitrile;hydrobromide

15. Nsc-758684

16. Citalopram (as Hydrobromide)

17. 1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-5-isobenzofurancarbonitrile Hydrobromide

18. I1e9d14f36

19. Cipram

20. (s)-1-(3-(dimethylamino)propyl)-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile Hydrobromide

21. Lu 10-171

22. Lu-10-171-b

23. Citalopram D4 Hbr

24. 59729-32-7 (hbr)

25. 1-(3-(dimethylamino)propyl)-1-(p-fluorophenyl)-5-phthalancarbonitrile Monohydrobromide

26. 5-isobenzofurancarbonitrile, 1-(3-(dimethylamino)propyl)-1-(4-fluorophenyl)-1,3-dihydro-, Monohydrobromide

27. Prepram Hbr

28. 1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-2-benzofuran-5-carbonitrile Hydrobromide

29. Smr000326936

30. Citalopram Hydrobromide [usan]

31. Lu-10-171

32. Sr-01000003129

33. 1-(3-(dimethylamino)propyl)-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile Monohydrobromide

34. Einecs 261-890-6

35. C20h21fn2o.hbr

36. Apertia

37. Prisdal

38. Lupram

39. Sepram

40. Unii-i1e9d14f36

41. 1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydroisobenzofuran-5-carbonitrile Hydrobromide

42. Citalopram Hydrobromide [usan:usp]

43. Celexa (tn)

44. Mfcd02101306

45. Cpd000326936

46. Schembl1118

47. Mls000758293

48. Mls000860078

49. Mls001401376

50. Mls002222294

51. Citalopram Hydrobromide (usp)

52. Citalopram Hydrobromide Solution

53. Chembl1200781

54. Dtxsid40872344

55. Pharmakon1600-01504172

56. Citalopram Hydrogen Bromide- Bio-x

57. Hy-b1287

58. Lu-10-171b

59. Citalopram Hydrobromide [mi]

60. Tox21_500258

61. Nsc758684

62. S4749

63. Zd 211

64. Zd-211

65. Citalopram Hydrobromide [hsdb]

66. Akos005145738

67. Ab10921

68. Ac-1595

69. Bcp9000537

70. Ccg-101022

71. Ccg-213271

72. Citalopram Hydrobromide [mart.]

73. Citalopram Hydrobromide [vandf]

74. Cs-4735

75. Ks-1043

76. Lp00258

77. Nc00272

78. Nsc 758684

79. Citalopram Hydrobromide [usp-rs]

80. Citalopram Hydrobromide [who-dd]

81. Ncgc00093717-01

82. Ncgc00093717-02

83. Ncgc00093717-03

84. Ncgc00260943-01

85. Bc164316

86. Citalopram Hydrobromide, >=98% (hplc)

87. Citalopram Hydrobromide [orange Book]

88. Eu-0100258

89. Ft-0600173

90. Citalopram Hydrobromide [ep Monograph]

91. Citalopram Hydrobromide [usp Impurity]

92. C 7861

93. C75790

94. Citalopram Hydrobromide [usp Monograph]

95. D00822

96. 729c327

97. A832439

98. Q-200865

99. Sr-01000003129-2

100. Sr-01000003129-4

101. W-105304

102. Citalopram Hydrobromide 100 Microg/ml In Acetonitrile

103. Q27280253

104. Sr-01000003129-10

105. Z1550648760

106. Citalopram Hydrobromide 0.1 Mg/ml In Methanol (as Free Base)

107. Citalopram Hydrobromide 1.0 Mg/ml In Methanol (as Free Base)

108. Citalopram Hydrobromide, European Pharmacopoeia (ep) Reference Standard

109. Citalopram Hydrobromide, United States Pharmacopeia (usp) Reference Standard

110. 1-(3-(dimethylamino)propyl)-1-(p-fluorophenyl)-5-phthalancarbonitrile Monohbr

111. Citalopram For System Suitability, European Pharmacopoeia (ep) Reference Standard

112. Citalopram Hydrobromide, Pharmaceutical Secondary Standard; Certified Reference Material

113. 1-(3-dimethylamino-propyl)-1-(4-fluoro-phenyl)-1,3-dihydro-isobenzofuran-5-carbonitrile Hydrobromide

114. 1-(3-dimethylaminopropyl)-1-(4'-fluorophenyl)-1, 3-dihydroisobenzofuran-5-carbonitrile Hbr

115. 1-(3-dimethylaminopropyl)-1-(4'-fluorophenyl)-1, 3-dihydroisobenzofuran-5-carbonitrile Hydrobromide

116. 1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-5-isobenzofurancarbonitril E Hydrobromide

117. 5-isobenzofurancarbonitrile, 1-(3-(dimethylamino)propyl)-1-(4-fluorophenyl)-1,3-dihydro-, Monohbr

118. 5-isobenzofurancarbonitrile, 1-[3-(dimethylamino)propyl]-1-(4-fluorophenyl)-1,3-dihydro-, Hydrobromide (1:1)

119. Citalopram Hydrobromide Solution, 1.0 Mg/ml In Methanol (as Free Base), Ampule Of 1 Ml, Certified Reference Material

120. Citalopram Hydrobromide Solution, 100 Mug/ml In Methanol (as Free Base), Ampule Of 1 Ml, Certified Reference Material

2.4 Create Date

2005-06-24

3 Chemical and Physical Properties

Molecular Formula	C₂₀H₂₂BrFN₂O
Molecular Weight	405.3 g/mol
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	4
Rotatable Bond Count	5
Exact Mass	404.08995 g/mol
Monoisotopic Mass	404.08995 g/mol
Topological Polar Surface Area	36.3 Å²
Heavy Atom Count	25
Formal Charge	0
Complexity	466
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
Undefined Atom Stereocenter Count	1
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
Covalently Bonded Unit Count	2

4 Drug and Medication Information

4.1 Drug Information

1 of 4
Drug Name	Celexa
Active Ingredient	Citalopram hydrobromide
Dosage Form	Tablet
Route	Oral
Strength	eq 40mg base; eq 20mg base; eq 10mg base
Market Status	Prescription
Company	Forest Labs

2 of 4
Drug Name	Citalopram hydrobromide
PubMed Health	Citalopram (By mouth)
Drug Classes	Antidepressant
Active Ingredient	Citalopram hydrobromide
Dosage Form	Tablet; Capsule; Solution
Route	orally disintegrating; Oral
Strength	eq 40mg base; eq 10mg base/5ml; eq 20mg base; eq 10mg base; 40mg
Market Status	Prescription
Company	Mylan Pharms; Glenmark Generics; Silarx; Amneal Pharms Ny; Teva Pharms; Epic Pharma; Apotex; Aurobindo; Aurobindo Pharma; Sun Pharm Inds; Torrent Pharms; Dr Reddys Labs; Pliva; Invagen Pharms; Cipla; Mylan; Roxane; Biovail Labs Intl

3 of 4
Drug Name	Celexa
Active Ingredient	Citalopram hydrobromide
Dosage Form	Tablet
Route	Oral
Strength	eq 40mg base; eq 20mg base; eq 10mg base
Market Status	Prescription
Company	Forest Labs

4 of 4
Drug Name	Citalopram hydrobromide
PubMed Health	Citalopram (By mouth)
Drug Classes	Antidepressant
Active Ingredient	Citalopram hydrobromide
Dosage Form	Tablet; Capsule; Solution
Route	orally disintegrating; Oral
Strength	eq 40mg base; eq 10mg base/5ml; eq 20mg base; eq 10mg base; 40mg
Market Status	Prescription
Company	Mylan Pharms; Glenmark Generics; Silarx; Amneal Pharms Ny; Teva Pharms; Epic Pharma; Apotex; Aurobindo; Aurobindo Pharma; Sun Pharm Inds; Torrent Pharms; Dr Reddys Labs; Pliva; Invagen Pharms; Cipla; Mylan; Roxane; Biovail Labs Intl

5 Pharmacology and Biochemistry

5.1 MeSH Pharmacological Classification

Selective Serotonin Reuptake Inhibitors

Compounds that specifically inhibit the reuptake of serotonin in the brain. (See all compounds classified as Selective Serotonin Reuptake Inhibitors.)

Antidepressive Agents, Second-Generation

A structurally and mechanistically diverse group of drugs that are not tricyclics or monoamine oxidase inhibitors. The most clinically important appear to act selectively on serotonergic systems, especially by inhibiting serotonin reuptake. (See all compounds classified as Antidepressive Agents, Second-Generation.)

5.2 FDA Pharmacological Classification

5.2.1 Pharmacological Classes

Serotonin Uptake Inhibitors [MoA]; Serotonin Reuptake Inhibitor [EPC]

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API Reference Price

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PHARMACEUTICAL","supplierCountry":"CHINA","foreign_port":"SHANGHAI","customer":"MEDREICH","customerCountry":"INDIA","quantity":"140.00","actualQuantity":"140","unit":"KGS","unitRateFc":"120","totalValueFC":"16972.6","currency":"USD","unitRateINR":"10134","date":"11-Jul-2024","totalValueINR":"1418760","totalValueInUsd":"16972.6","indian_port":"Bangalore Air","hs_no":"29329990","bill_no":"4448823","productDescription":"API","marketType":"REGULATED MARKET","country":"CHINA","selfForZScoreResived":"Pharma Grade","supplierPort":"SHANGHAI","supplierAddress":"LTD. XUNQIAO, LINHAIZHEJIANG 317024SDNF CHINA","customerAddress":"MEDREICH HOUSE, NO12\/8,"},{"dataSource":"API Import","activeIngredients":"","year":"2024","qtr":"Q3","strtotime":1722364200,"product":"CITALOPRAM HYDROBROMIDE","address":"MEDREICH HOUSE, NO12\/8,","city":"SEVA NAGAR, BANGALORE, KARNATAKA","supplier":"ZHEJIANG HUAHAI PHARMACEUTICAL","supplierCountry":"CHINA","foreign_port":"SHANGHAI","customer":"MEDREICH","customerCountry":"INDIA","quantity":"25.00","actualQuantity":"25","unit":"KGS","unitRateFc":"115","totalValueFC":"2908","currency":"USD","unitRateINR":"9723.3","date":"31-Jul-2024","totalValueINR":"243081.25","totalValueInUsd":"2908","indian_port":"Madras Sea","hs_no":"29329990","bill_no":"4800643","productDescription":"API","marketType":"REGULATED MARKET","country":"CHINA","selfForZScoreResived":"Pharma Grade","supplierPort":"SHANGHAI","supplierAddress":"LTD. XUNQIAO, LINHAIZHEJIANG 317024SDNF CHINA","customerAddress":"MEDREICH HOUSE, NO12\/8,"},{"dataSource":"API Import","activeIngredients":"","year":"2024","qtr":"Q3","strtotime":1722364200,"product":"CITALOPRAM HYDROBROMIDE","address":"MEDREICH HOUSE, NO12\/8,","city":"SEVA NAGAR, BANGALORE, KARNATAKA","supplier":"ZHEJIANG HUAHAI PHARMACEUTICAL","supplierCountry":"CHINA","foreign_port":"SHANGHAI","customer":"MEDREICH","customerCountry":"INDIA","quantity":"275.00","actualQuantity":"275","unit":"KGS","unitRateFc":"115","totalValueFC":"31987.8","currency":"USD","unitRateINR":"9723.3","date":"31-Jul-2024","totalValueINR":"2673893.75","totalValueInUsd":"31987.8","indian_port":"Madras Sea","hs_no":"29329990","bill_no":"4800643","productDescription":"API","marketType":"REGULATED MARKET","country":"CHINA","selfForZScoreResived":"Pharma Grade","supplierPort":"SHANGHAI","supplierAddress":"LTD. XUNQIAO, LINHAIZHEJIANG 317024SDNF CHINA","customerAddress":"MEDREICH HOUSE, NO12\/8,"},{"dataSource":"API Import","activeIngredients":"","year":"2024","qtr":"Q3","strtotime":1723573800,"product":"CITALOPRAM HYDROBROMIDE (QTY: 1 X 200MG, VALUE USD: 530) (FOC)","address":"P.NO. D6 D8, SY.NO. 234\/2,234\/3,","city":"TURKAPALLY(V),SHAMEERPET, HYDERABAD","supplier":"UNITED STATES PHARMACOPEIAL","supplierCountry":"INDIA","foreign_port":"WASHINGTON, DULLES I","customer":"UNITED STATES PHARMACOPEIA - INDIA PRIVATE LIMITED","customerCountry":"INDIA","quantity":"0.00","actualQuantity":"0.0002","unit":"KGS","unitRateFc":"2650000","totalValueFC":"553.1","currency":"USD","unitRateINR":"231948200","date":"14-Aug-2024","totalValueINR":"46389.64","totalValueInUsd":"553.1","indian_port":"Hyderabad Air","hs_no":"29329990","bill_no":"5055144","productDescription":"Re-Import","marketType":"REGULATED MARKET","country":"INDIA","selfForZScoreResived":"Pharma Grade","supplierPort":"WASHINGTON, DULLES I","supplierAddress":"7135 ENGLISH MUFFIN WAY FREDERICK,MD,US 21704,UNITED STATES OF AMERICASDNF United States","customerAddress":"P.NO. D6 D8, SY.NO. 234\/2,234\/3,"}]

Number of Transactions

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Quantity (KGS) & Unit rate (USD/KGS) over time

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Importing Country	Total Quantity (KGS)	Average Price (USD/KGS)	Number of Transactions

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DOSAGE - TABLET;ORAL - EQ 10MG BASE

USFDA APPLICATION NUMBER - 20822

DOSAGE - TABLET;ORAL - EQ 20MG BASE

USFDA APPLICATION NUMBER - 20822

DOSAGE - TABLET;ORAL - EQ 40MG BASE

USFDA APPLICATION NUMBER - 20822

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ABOUT THIS PAGE

Citalopram Hydrobromide Manufacturers

A Citalopram Hydrobromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Citalopram Hydrobromide, including repackagers and relabelers. The FDA regulates Citalopram Hydrobromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Citalopram Hydrobromide 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 Citalopram Hydrobromide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Citalopram Hydrobromide Suppliers

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

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

Citalopram Hydrobromide USDMF

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

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

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

Citalopram Hydrobromide CEP

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

A Citalopram Hydrobromide CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Citalopram Hydrobromide 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 Citalopram Hydrobromide suppliers with CEP (COS) on PharmaCompass.

Citalopram Hydrobromide WC

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

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

Citalopram Hydrobromide 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 Citalopram Hydrobromide as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Citalopram Hydrobromide 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 Citalopram Hydrobromide 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 Citalopram Hydrobromide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Citalopram Hydrobromide NDC to their finished compounded human drug products, they may choose to do so.

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

Citalopram Hydrobromide GMP

Citalopram Hydrobromide 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 Citalopram Hydrobromide 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 Citalopram Hydrobromide GMP manufacturer or Citalopram Hydrobromide GMP API supplier for your needs.

Citalopram Hydrobromide CoA

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

Citalopram Hydrobromide CoA mostly includes findings from lab analyses of a specific batch. For each Citalopram Hydrobromide 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.

Citalopram Hydrobromide may be tested according to a variety of international standards, such as European Pharmacopoeia (Citalopram Hydrobromide EP), Citalopram Hydrobromide JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Citalopram Hydrobromide 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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DRUG PRODUCT COMPOSITIONS

TABLET;ORAL - EQ 10MG BASE

TABLET;ORAL - EQ 20MG BASE

TABLET;ORAL - EQ 40MG BASE

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