Synopsis
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KDMF
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VMF
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1. Alotec
2. Alupent
3. Astmopent
4. Metaprel
5. Metaproterenol
6. Metaproterenol Polistirex
7. Orciprenaline
8. Orciprenaline Sulfate
9. Polistirex, Metaproterenol
1. Orciprenaline Sulfate
2. 5874-97-5
3. Metaproterenol Hemisulfate
4. Metaproterenol Hemisulfate Salt
5. Metaproterenol Sulphate
6. Orciprenaline Sulphate
7. Alupent
8. Prometa
9. Orciprenaline (hemisulfate)
10. Metaproterenol (hemisulfate)
11. Th-152
12. Metaproterenol Sulfate, Orciprenaline Sulfate
13. 5-[1-hydroxy-2-(propan-2-ylamino)ethyl]benzene-1,3-diol;sulfuric Acid
14. Dsstox_cid_25391
15. Dsstox_rid_80848
16. Dsstox_gsid_45391
17. Gj20h50yf0
18. Metaproterenol Sulfate [usan]
19. Prestwick_845
20. Alupent (tn)
21. Ncgc00016662-01
22. Cas-5874-97-5
23. Schembl41815
24. Metaproterenol Sulfate (usp)
25. Orciprenaline Sulfate (jp17)
26. Chembl1568057
27. Dtxsid4045391
28. Hms1569f11
29. Hms2096f11
30. Hms3262c10
31. Hms3713f11
32. Metaproterenol Sulfate [mi]
33. Orciprenaline Sulfate [jan]
34. Bcp13601
35. Orciprenaline For System Suitability
36. Tox21_110551
37. Tox21_500734
38. Metaproterenol Sulfate [vandf]
39. Orciprenaline Sulfate [mart.]
40. Akos015994757
41. Orciprenaline Sulfate [who-dd]
42. Tox21_110551_1
43. Ccg-220505
44. Ccg-222038
45. Lp00734
46. Metaproterenol Sulfate [usp-rs]
47. Ss-4263
48. Ncgc00015655-09
49. Ncgc00094078-01
50. Ncgc00261419-01
51. Db-053257
52. Metaproterenol Sulfate [orange Book]
53. Orciprenaline Sulfate [ep Monograph]
54. Eu-0100734
55. Ft-0628263
56. Sw198971-2
57. En300-50867
58. Metaproterenol Sulfate [usp Monograph]
59. D00685
60. M 2398
61. 874m975
62. Metaproterenol Sulfate;th-152; Th 152; Th152
63. Sr-01000872665
64. Sr-01000872665-1
65. Metaproterenol Hemisulfate 100 Microg/ml In Methanol
66. Q27279120
67. Z955123630
68. 5-(1-hydroxy-2-(isopropylamino)ethyl)benzene-1,3-diol Hemisulfate
69. Bis(5-(1-hydroxy-2-(isopropylamino)ethyl)benzene-1,3-diol) Sulfate
70. Metaproterenol Sulfate, United States Pharmacopeia (usp) Reference Standard
71. Orciprenaline Sulfate, European Pharmacopoeia (ep) Reference Standard
72. (+/-)-3,5-dihydroxy-.alpha.-((isopropylamino)methyl)benzyl Alcohol Sulfate (2:1)
73. (+/-)-3,5-dihydroxy-.alpha.-((isopropylamino)methyl)benzyl Alcohol Sulphate (2:1)
74. Bis(5-{1-hydroxy-2-[(propan-2-yl)amino]ethyl}benzene-1,3-diol); Sulfuric Acid
75. Orciprenaline For System Suitability, European Pharmacopoeia (ep) Reference Standard
76. 1,3-benzenediol, 5-(1-hydroxy-2-(1-methylethyl)amino)ethyl-, (+/-)-, Sulfate (2:1) (salt)
77. 1,3-benzenediol, 5-(1-hydroxy-2-(1-methylethyl)amino)ethyl-, (+/-)-, Sulphate (2:1) (salt)
Molecular Weight | 520.6 g/mol |
---|---|
Molecular Formula | C22H36N2O10S |
Hydrogen Bond Donor Count | 10 |
Hydrogen Bond Acceptor Count | 12 |
Rotatable Bond Count | 8 |
Exact Mass | 520.20906652 g/mol |
Monoisotopic Mass | 520.20906652 g/mol |
Topological Polar Surface Area | 228 Ų |
Heavy Atom Count | 35 |
Formal Charge | 0 |
Complexity | 258 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 2 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 3 |
1 of 2 | |
---|---|
Drug Name | Metaproterenol sulfate |
Drug Label | Metaproterenol sulfate syrup is an oral bronchodilator. Each teaspoonful (5 mL), for oral administration, contains metaproterenol sulfate 10 mg. In addition, each teaspoonful (5 mL) contains the following inactive ingredients:citric acid, edetate dis... |
Active Ingredient | Metaproterenol sulfate |
Dosage Form | Tablet; Syrup; Solution |
Route | Oral; Inhalation |
Strength | 10mg/5ml; 0.4%; 0.6%; 10mg; 20mg |
Market Status | Prescription |
Company | Wockhardt; Silarx; Mylan Speclt; Par Pharm |
2 of 2 | |
---|---|
Drug Name | Metaproterenol sulfate |
Drug Label | Metaproterenol sulfate syrup is an oral bronchodilator. Each teaspoonful (5 mL), for oral administration, contains metaproterenol sulfate 10 mg. In addition, each teaspoonful (5 mL) contains the following inactive ingredients:citric acid, edetate dis... |
Active Ingredient | Metaproterenol sulfate |
Dosage Form | Tablet; Syrup; Solution |
Route | Oral; Inhalation |
Strength | 10mg/5ml; 0.4%; 0.6%; 10mg; 20mg |
Market Status | Prescription |
Company | Wockhardt; Silarx; Mylan Speclt; Par Pharm |
Tocolytic Agents
Drugs that prevent preterm labor and immature birth by suppressing uterine contractions (TOCOLYSIS). Agents used to delay premature uterine activity include magnesium sulfate, beta-mimetics, oxytocin antagonists, calcium channel inhibitors, and adrenergic beta-receptor agonists. The use of intravenous alcohol as a tocolytic is now obsolete. (See all compounds classified as Tocolytic Agents.)
Bronchodilator Agents
Agents that cause an increase in the expansion of a bronchus or bronchial tubes. (See all compounds classified as Bronchodilator Agents.)
Adrenergic beta-2 Receptor Agonists
Compounds bind to and activate ADRENERGIC BETA-2 RECEPTORS. (See all compounds classified as Adrenergic beta-2 Receptor Agonists.)
Sympathomimetics
Drugs that mimic the effects of stimulating postganglionic adrenergic sympathetic nerves. Included here are drugs that directly stimulate adrenergic receptors and drugs that act indirectly by provoking the release of adrenergic transmitters. (See all compounds classified as Sympathomimetics.)
Related Excipient Companies
Excipients by Applications
Market Place
REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A METAPROTERENOL SULFATE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of METAPROTERENOL SULFATE, including repackagers and relabelers. The FDA regulates METAPROTERENOL SULFATE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. METAPROTERENOL SULFATE 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 METAPROTERENOL SULFATE manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A METAPROTERENOL SULFATE supplier is an individual or a company that provides METAPROTERENOL SULFATE active pharmaceutical ingredient (API) or METAPROTERENOL SULFATE finished formulations upon request. The METAPROTERENOL SULFATE suppliers may include METAPROTERENOL SULFATE API manufacturers, exporters, distributors and traders.
click here to find a list of METAPROTERENOL SULFATE suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A METAPROTERENOL SULFATE DMF (Drug Master File) is a document detailing the whole manufacturing process of METAPROTERENOL SULFATE active pharmaceutical ingredient (API) in detail. Different forms of METAPROTERENOL SULFATE DMFs exist exist since differing nations have different regulations, such as METAPROTERENOL SULFATE USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A METAPROTERENOL SULFATE DMF submitted to regulatory agencies in the US is known as a USDMF. METAPROTERENOL SULFATE USDMF includes data on METAPROTERENOL SULFATE's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The METAPROTERENOL SULFATE USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of METAPROTERENOL SULFATE suppliers with USDMF on PharmaCompass.
A METAPROTERENOL SULFATE CEP of the European Pharmacopoeia monograph is often referred to as a METAPROTERENOL SULFATE Certificate of Suitability (COS). The purpose of a METAPROTERENOL SULFATE CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of METAPROTERENOL SULFATE EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of METAPROTERENOL SULFATE to their clients by showing that a METAPROTERENOL SULFATE CEP has been issued for it. The manufacturer submits a METAPROTERENOL SULFATE CEP (COS) as part of the market authorization procedure, and it takes on the role of a METAPROTERENOL SULFATE CEP holder for the record. Additionally, the data presented in the METAPROTERENOL SULFATE CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the METAPROTERENOL SULFATE DMF.
A METAPROTERENOL SULFATE CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. METAPROTERENOL SULFATE 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 METAPROTERENOL SULFATE suppliers with CEP (COS) on PharmaCompass.
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 METAPROTERENOL SULFATE as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for METAPROTERENOL SULFATE API and other APIs are published in this directory by the FDA.
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 METAPROTERENOL SULFATE 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.
The NDC directory also contains data on finished compounded human drug products that contain METAPROTERENOL SULFATE and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a METAPROTERENOL SULFATE NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of METAPROTERENOL SULFATE suppliers with NDC on PharmaCompass.
METAPROTERENOL SULFATE 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 METAPROTERENOL SULFATE 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 METAPROTERENOL SULFATE GMP manufacturer or METAPROTERENOL SULFATE GMP API supplier for your needs.
A METAPROTERENOL SULFATE CoA (Certificate of Analysis) is a formal document that attests to METAPROTERENOL SULFATE's compliance with METAPROTERENOL SULFATE specifications and serves as a tool for batch-level quality control.
METAPROTERENOL SULFATE CoA mostly includes findings from lab analyses of a specific batch. For each METAPROTERENOL SULFATE 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.
METAPROTERENOL SULFATE may be tested according to a variety of international standards, such as European Pharmacopoeia (METAPROTERENOL SULFATE EP), METAPROTERENOL SULFATE JP (Japanese Pharmacopeia) and the US Pharmacopoeia (METAPROTERENOL SULFATE USP).
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