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1. Altramet
2. Biomet
3. Biomet400
4. Cimetidine
5. Cimetidine Hcl
6. Eureceptor
7. Hcl, Cimetidine
8. Histodil
9. Hydrochloride, Cimetidine
10. N-cyano-n'-methyl-n''-(2-(((5-methyl-1h-imidazol-4-yl)methyl)thio)ethyl)guanidine
11. Sk And F 92334
12. Sk And F-92334
13. Sk And F92334
14. Skf 92334
15. Skf-92334
16. Skf92334
17. Tagamet
1. 70059-30-2
2. Cimetidine Hcl
3. Cimetidinehydrochloride
4. Cimetidine (hydrochloride)
5. Cimetex
6. 2-cyano-1-methyl-3-(2-(((5-methylimidazol-4-yl)methyl)thio)ethyl)guanidine Monohydrochloride
7. N-cyano-n'-methyl-n''-[2-[[(5-methyl-1h-imidazol-4-yl)methyl]thio]ethyl]guanidine Hydrochloride
8. Endo
9. Tagamet Liquid
10. Wf10491673
11. Tagamet Injection
12. Guanidine, N''-cyano-n-methyl-n'-(2-(((5-methyl-1h-imidazol-4-yl)methyl)thio)ethyl)-, Monohydrochloride
13. Chebi:50362
14. N-cyano-n'-methyl-n''-(2-(((5-methyl-1h-imidazol-4-yl)methyl)thio)ethyl)guanidine Hydrochloride
15. Cimetidine Hydrochloride [usan]
16. Einecs 274-297-2
17. Unii-wf10491673
18. Einecs 276-264-8
19. Cimetidine Hydrochloride [usan:usp]
20. 71989-90-7
21. Schembl42142
22. Schembl42144
23. Cimetidine Hydrochloride (tn)
24. Cimetidine Hydrochloride (usp)
25. Chembl1201051
26. Schembl11156749
27. Dtxsid10990302
28. Cimetidine Hydrochloride [mi]
29. Cimetidine Hydrochloride In Sodium Chloride 0.9% In Plastic Container
30. Hy-14289a
31. Mfcd01724314
32. Tagamet Hydrochloride In Sodium Chloride 0.9% In Plastic Container
33. Akos015961108
34. Akos037643350
35. Ac-4278
36. Cimetidine Hydrochloride [mart.]
37. Cimetidine Hydrochloride [vandf]
38. Cimetidine Hydrochloride [usp-rs]
39. Cimetidine Hydrochloride [who-dd]
40. 1-cyano-2-methyl-3-[2-[(5-methyl-1h-imidazol-4-yl)methylsulfanyl]ethyl]guanidine;hydrochloride
41. As-15040
42. Guanidine, N'-cyano-n-methyl-n'-(2-(((5-methyl-1h-imidazol-4-yl)methyl)thio)ethyl)-, Monohydrochloride
43. N-cyano-n'-methyl-n''-(2-(((5-methyl-1h-imidazol-4-yl)methyl)thio)ethyl)guanidine Monohydrochloride
44. Db-055373
45. Cs-0031039
46. Ft-0602954
47. Cimetidine Hydrochloride [orange Book]
48. Cimetidine Hydrochloride [ep Monograph]
49. Cimetidine Hydrochloride [usp Monograph]
50. D03503
51. 059c302
52. A923492
53. W-104570
54. Q27122038
55. Cimetidine Hydrochloride, Pharmaceutical Secondary Standard; Certified Reference Material
56. Cimetidine Hydrochloride, United States Pharmacopeia (usp) Reference Standard
57. Cimetidine Hydrochloride, European Pharmacopoeia (ep) Reference Standard, European Pharmacopoeia (ep) Reference Standard
58. Guanidine, N-cyano-n'-methyl-n''-[2-[[(5-methyl-1h-imidazol-4-yl)methyl]thio]ethyl]-, Monohydrochloride
59. N-cyano-n''-methyl-n'-(2-{[(4-methyl-1h-imidazol-5-yl)methyl]sulfanyl}ethyl)guanidine--hydrogen Chloride (1/1)
Molecular Weight | 288.80 g/mol |
---|---|
Molecular Formula | C10H17ClN6S |
Hydrogen Bond Donor Count | 4 |
Hydrogen Bond Acceptor Count | 4 |
Rotatable Bond Count | 7 |
Exact Mass | 288.0923934 g/mol |
Monoisotopic Mass | 288.0923934 g/mol |
Topological Polar Surface Area | 114 Ų |
Heavy Atom Count | 18 |
Formal Charge | 0 |
Complexity | 296 |
Isotope Atom Count | 0 |
Defined Atom Stereocenter Count | 0 |
Undefined Atom Stereocenter Count | 0 |
Defined Bond Stereocenter Count | 0 |
Undefined Bond Stereocenter Count | 0 |
Covalently Bonded Unit Count | 2 |
1 of 2 | |
---|---|
Drug Name | Cimetidine hydrochloride |
Drug Label | Cimetidine is a histamine H2 receptor-antagonist. Chemically it is N"-cyano-N-methyl-N'-[2-[[(5-methyl-1H-imidazol-4-yl)methyl]thio]-ethyl]-guanidine.The molecular formula for cimetidine hydrochloride is C10H16N6S HCl and the molecular weight i |
Active Ingredient | Cimetidine hydrochloride |
Dosage Form | Injectable; Solution |
Route | Injection; Oral |
Strength | eq 300mg base/2ml; eq 300mg base/5ml |
Market Status | Prescription |
Company | Wockhardt; Hi Tech Pharma; Ani Pharms; Pharm Assoc; Dava Pharms |
2 of 2 | |
---|---|
Drug Name | Cimetidine hydrochloride |
Drug Label | Cimetidine is a histamine H2 receptor-antagonist. Chemically it is N"-cyano-N-methyl-N'-[2-[[(5-methyl-1H-imidazol-4-yl)methyl]thio]-ethyl]-guanidine.The molecular formula for cimetidine hydrochloride is C10H16N6S HCl and the molecular weight i |
Active Ingredient | Cimetidine hydrochloride |
Dosage Form | Injectable; Solution |
Route | Injection; Oral |
Strength | eq 300mg base/2ml; eq 300mg base/5ml |
Market Status | Prescription |
Company | Wockhardt; Hi Tech Pharma; Ani Pharms; Pharm Assoc; Dava Pharms |
Cytochrome P-450 CYP1A2 Inhibitors
Drugs and compounds which inhibit or antagonize the biosynthesis or actions of CYTOCHROME P-450 CYP1A2. (See all compounds classified as Cytochrome P-450 CYP1A2 Inhibitors.)
Anti-Ulcer Agents
Various agents with different action mechanisms used to treat or ameliorate PEPTIC ULCER or irritation of the gastrointestinal tract. This has included ANTIBIOTICS to treat HELICOBACTER INFECTIONS; HISTAMINE H2 ANTAGONISTS to reduce GASTRIC ACID secretion; and ANTACIDS for symptomatic relief. (See all compounds classified as Anti-Ulcer Agents.)
Histamine H2 Antagonists
Drugs that selectively bind to but do not activate histamine H2 receptors, thereby blocking the actions of histamine. Their clinically most important action is the inhibition of acid secretion in the treatment of gastrointestinal ulcers. Smooth muscle may also be affected. Some drugs in this class have strong effects in the central nervous system, but these actions are not well understood. (See all compounds classified as Histamine H2 Antagonists.)
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REF. STANDARDS & IMPURITIES
ABOUT THIS PAGE
A Cimetidine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cimetidine Hydrochloride, including repackagers and relabelers. The FDA regulates Cimetidine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cimetidine Hydrochloride 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 Cimetidine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cimetidine Hydrochloride supplier is an individual or a company that provides Cimetidine Hydrochloride active pharmaceutical ingredient (API) or Cimetidine Hydrochloride finished formulations upon request. The Cimetidine Hydrochloride suppliers may include Cimetidine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Cimetidine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Cimetidine Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Cimetidine Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Cimetidine Hydrochloride DMFs exist exist since differing nations have different regulations, such as Cimetidine Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Cimetidine Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Cimetidine Hydrochloride USDMF includes data on Cimetidine Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Cimetidine Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Cimetidine Hydrochloride suppliers with USDMF 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 Cimetidine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Cimetidine Hydrochloride 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 Cimetidine Hydrochloride 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 Cimetidine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Cimetidine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Cimetidine Hydrochloride suppliers with NDC on PharmaCompass.
Cimetidine Hydrochloride 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 Cimetidine Hydrochloride 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 Cimetidine Hydrochloride GMP manufacturer or Cimetidine Hydrochloride GMP API supplier for your needs.
A Cimetidine Hydrochloride CoA (Certificate of Analysis) is a formal document that attests to Cimetidine Hydrochloride's compliance with Cimetidine Hydrochloride specifications and serves as a tool for batch-level quality control.
Cimetidine Hydrochloride CoA mostly includes findings from lab analyses of a specific batch. For each Cimetidine Hydrochloride 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.
Cimetidine Hydrochloride may be tested according to a variety of international standards, such as European Pharmacopoeia (Cimetidine Hydrochloride EP), Cimetidine Hydrochloride JP (Japanese Pharmacopeia) and the US Pharmacopoeia (Cimetidine Hydrochloride USP).
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