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Chemistry

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Also known as: Ranitidine hydrochloride, 66357-59-3, 71130-06-8, Fendibina, Gastridina, Gastrolav
Molecular Formula
C13H23ClN4O3S
Molecular Weight
350.87  g/mol
InChI Key
GGWBHVILAJZWKJ-KJEVSKRMSA-N

Ranitidine Hydrochloride
A non-imidazole blocker of those histamine receptors that mediate gastric secretion (H2 receptors). It is used to treat gastrointestinal ulcers.
1 2D Structure

Ranitidine Hydrochloride

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
(E)-1-N'-[2-[[5-[(dimethylamino)methyl]furan-2-yl]methylsulfanyl]ethyl]-1-N-methyl-2-nitroethene-1,1-diamine;hydrochloride
2.1.2 InChI
InChI=1S/C13H22N4O3S.ClH/c1-14-13(9-17(18)19)15-6-7-21-10-12-5-4-11(20-12)8-16(2)3;/h4-5,9,14-15H,6-8,10H2,1-3H3;1H/b13-9+;
2.1.3 InChI Key
GGWBHVILAJZWKJ-KJEVSKRMSA-N
2.1.4 Canonical SMILES
CNC(=C[N+](=O)[O-])NCCSCC1=CC=C(O1)CN(C)C.Cl
2.1.5 Isomeric SMILES
CN/C(=C\[N+](=O)[O-])/NCCSCC1=CC=C(O1)CN(C)C.Cl
2.2 Synonyms
2.2.1 MeSH Synonyms

1. Ah 19065

2. Ah-19065

3. Ah19065

4. Biotidin

5. Hydrochloride, Ranitidine

6. N (2-(((5-((dimethylamino)methyl)-2-furanyl)methyl)thio)ethyl)-n'-methyl-2-nitro-1,1-ethenediamine

7. Ranisen

8. Ranitidin

9. Ranitidine

10. Ranitidine Hydrochloride

11. Sostril

12. Zantac

13. Zantic

2.2.2 Depositor-Supplied Synonyms

1. Ranitidine Hydrochloride

2. 66357-59-3

3. 71130-06-8

4. Fendibina

5. Gastridina

6. Gastrolav

7. Kuracid

8. Raniberl

9. Ranibloc

10. Alquen

11. Rani-nerton

12. Zantac

13. Nu-ranit

14. Rani-q

15. Ranitidine (hydrochloride)

16. Santanol

17. Tanidina

18. Toriol

19. Coralen

20. Quantor

21. Radin

22. Chebi:8777

23. Gastrial

24. Raniben

25. Ranibeta

26. Azantac

27. Zantac (tn)

28. (e)-1-n'-[2-[[5-[(dimethylamino)methyl]furan-2-yl]methylsulfanyl]ethyl]-1-n-methyl-2-nitroethene-1,1-diamine;hydrochloride

29. Mfcd00941509

30. {2-[({5-[(dimethylamino)methyl]furan-2-yl}methyl)sulfanyl]ethyl}[(z)-1-(methylamino)-2-nitroethenyl]amine Hydrochloride

31. Smr000653467

32. (e)-n-(2-(((5-((dimethylamino)methyl)furan-2-yl)methyl)thio)ethyl)-n-methyl-2-nitroethene-1,1-diamine

33. N-(2-((5-((dimethylamino)methyl)furfuryl)thio)ethyl)-n'-methyl-2-nitrovinylidenediamine Monohydrochloride

34. C13h22n4o3s.hcl

35. Zantic

36. Zantac;noctone

37. Sr-01000075288

38. Ah19065

39. Ah-19065

40. Prestwick_635

41. Einecs 275-207-4

42. Ranitidine (zantac)

43. Ranitidine Hydrochloride 100 Microg/ml In Acetonitrile

44. Epitope Id:127516

45. Mls001146938

46. Mls002548856

47. Chembl1092473

48. Hy-b0281a

49. Hms1568j03

50. Amy24712

51. Bcp28420

52. N-[2-[[[5-[(dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-n'-methyl-2-nitro-1,1-ethenediamine Hydrochloride

53. N-[2-[5-[(dimethylamino)methyl]furfurylthio]ethyl]-n'-methyl-2-nitro-1,1-ethenediamine Hydrochloride

54. Tox21_501073

55. S1801

56. Ranitidine Hydrochloride (jp17/usp)

57. Akos015895250

58. Ccg-212946

59. Lp01073

60. Nc00479

61. Ranitidine For Impurity A Identification

62. Ncgc00094351-01

63. Ncgc00261758-01

64. Ac-12743

65. N-[2-[[5-(dimethylaminomethyl)furan-2-yl]methylsulfanyl]ethyl]-n'-methyl-2-nitroethene-1,1-diamine Hydrochloride

66. Eu-0101073

67. R-101

68. R0073

69. Sw196800-3

70. Bim-0051043.0001

71. D00673

72. 357n593

73. A835435

74. Sr-01000075288-2

75. W-104534

76. (e)-n-(2-(((5-((dimethylamino)methyl)furan-2-yl)methyl)thio)ethyl)-n'-methyl-2-nitroethene-1,1-diamine Hydrochloride

77. (e)-n1'-[2-[[5-[(dimethylamino)methyl]-2-furanyl]methylthio]ethyl]-n1-methyl-2-nitroethene-1,1-diamine Hydrochloride

78. (e)-n1'-[2-[[5-[(dimethylamino)methyl]furan-2-yl]methylsulfanyl]ethyl]-n1-methyl-2-nitro-ethene-1,1-diamine Hydrochloride

79. 1,1-ethenediamine, N-(2-(((5-((dimethylamino)methyl)-2-furanyl)methyl)thio)ethyl)-n'-methyl-2-nitro-, Hydrochloride

80. N-(2-(((5-((dimethylamino)methyl)furan-2-yl)methyl)thio)ethyl)-n'-methyl-2-nitroethene-1,1-diamine Hydrochloride

81. N-(2-(((5-((dimethylamino)methyl)furan-2-yl)methyl)thio)ethyl)-n-methyl-2-nitroethene-1,1-diaminehydrochloride

82. N-(2-((5-(dimethylaminomethyl)furan-2-yl)methylsulfanyl)ethyl)-n'-methyl-2-nitroethene-1,1-diamine Hcl

83. N-[2-[[[5-[(dimethylamino)methyl]-2 -furanyl]methyl]thio]ethyl]-n'-methyl-2-nitro-1,1-e Thanediamine Hydrochloride

2.3 Create Date
2005-06-24
3 Chemical and Physical Properties
Molecular Weight 350.87 g/mol
Molecular Formula C13H23ClN4O3S
Hydrogen Bond Donor Count3
Hydrogen Bond Acceptor Count7
Rotatable Bond Count9
Exact Mass350.1179395 g/mol
Monoisotopic Mass350.1179395 g/mol
Topological Polar Surface Area112 Ų
Heavy Atom Count22
Formal Charge0
Complexity347
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count1
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count2
4 Drug and Medication Information
4.1 Drug Information
1 of 10  
Drug NameRanitidine hydrochloride
Active IngredientRanitidine hydrochloride
Dosage FormTablet; Syrup; Capsule; Injectable
RouteInjection; Oral
Strengtheq 150mg base; eq 15mg base/ml; eq 75mg base; 25mg/ml; eq 300mg base; eq 25mg base/ml
Market StatusOver the Counter; Prescription
CompanyVintage Pharms; Amneal Pharms; Wockhardt; Silarx; Breckenridge Pharm; Teva; Pharm Assoc; Apotex; Torpharm; Shasun Chems; Taro; Sandoz; Par Pharm; Perrigo R And D; Svads Holdings Sa; Glenmark Generics; Amneal Pharms Ny; Ivax Sub Teva Pharms; Hi Tech Pharma

2 of 10  
Drug NameZantac
PubMed HealthRanitidine (Injection)
Drug ClassesAntiulcer, Gastric Acid Secretion Inhibitor
Drug LabelThe active ingredient in ZANTAC 150 Tablets, ZANTAC 300 Tablets, and ZANTAC Syrup is ranitidine hydrochloride (HCl), USP, a histamine H2-receptor antagonist. Chemically it is N[2-[[[5-[(dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N-methyl-2...
Active IngredientRanitidine hydrochloride
Dosage FormSyrup; Injectable
RouteInjection; Oral
Strengtheq 15mg base/ml; eq 25mg base/ml
Market StatusPrescription
CompanyCovis Injectables; Glaxo Grp

3 of 10  
Drug NameZantac 150
PubMed HealthRanitidine
Drug ClassesAntiulcer, Gastric Acid Secretion Inhibitor
Drug LabelThe active ingredient in ZANTAC 150 Tablets, ZANTAC 300 Tablets, and ZANTAC Syrup is ranitidine hydrochloride (HCl), USP, a histamine H2-receptor antagonist. Chemically it is N[2-[[[5-[(dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N-methyl-2...
Active IngredientRanitidine hydrochloride
Dosage FormTablet
RouteOral
Strengtheq 150mg base
Market StatusOver the Counter; Prescription
CompanyBoehringer Ingelheim; Glaxo Grp

4 of 10  
Drug NameZantac 300
Active IngredientRanitidine hydrochloride
Dosage FormTablet
RouteOral
Strengtheq 300mg base
Market StatusPrescription
CompanyGlaxo Grp

5 of 10  
Drug NameZantac 75
Drug LabelThe active ingredient in ZANTAC 150 Tablets, ZANTAC 300 Tablets, and ZANTAC Syrup is ranitidine hydrochloride (HCl), USP, a histamine H2-receptor antagonist. Chemically it is N[2-[[[5-[(dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N-methyl-2...
Active IngredientRanitidine hydrochloride
Dosage FormTablet
RouteOral
Strengtheq 75mg base
Market StatusOver the Counter
CompanyBoehringer Ingelheim

6 of 10  
Drug NameRanitidine hydrochloride
Active IngredientRanitidine hydrochloride
Dosage FormTablet; Syrup; Capsule; Injectable
RouteInjection; Oral
Strengtheq 150mg base; eq 15mg base/ml; eq 75mg base; 25mg/ml; eq 300mg base; eq 25mg base/ml
Market StatusOver the Counter; Prescription
CompanyVintage Pharms; Amneal Pharms; Wockhardt; Silarx; Breckenridge Pharm; Teva; Pharm Assoc; Apotex; Torpharm; Shasun Chems; Taro; Sandoz; Par Pharm; Perrigo R And D; Svads Holdings Sa; Glenmark Generics; Amneal Pharms Ny; Ivax Sub Teva Pharms; Hi Tech Pharma

7 of 10  
Drug NameZantac
PubMed HealthRanitidine (Injection)
Drug ClassesAntiulcer, Gastric Acid Secretion Inhibitor
Drug LabelThe active ingredient in ZANTAC 150 Tablets, ZANTAC 300 Tablets, and ZANTAC Syrup is ranitidine hydrochloride (HCl), USP, a histamine H2-receptor antagonist. Chemically it is N[2-[[[5-[(dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N-methyl-2...
Active IngredientRanitidine hydrochloride
Dosage FormSyrup; Injectable
RouteInjection; Oral
Strengtheq 15mg base/ml; eq 25mg base/ml
Market StatusPrescription
CompanyCovis Injectables; Glaxo Grp

8 of 10  
Drug NameZantac 150
PubMed HealthRanitidine
Drug ClassesAntiulcer, Gastric Acid Secretion Inhibitor
Drug LabelThe active ingredient in ZANTAC 150 Tablets, ZANTAC 300 Tablets, and ZANTAC Syrup is ranitidine hydrochloride (HCl), USP, a histamine H2-receptor antagonist. Chemically it is N[2-[[[5-[(dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N-methyl-2...
Active IngredientRanitidine hydrochloride
Dosage FormTablet
RouteOral
Strengtheq 150mg base
Market StatusOver the Counter; Prescription
CompanyBoehringer Ingelheim; Glaxo Grp

9 of 10  
Drug NameZantac 300
Active IngredientRanitidine hydrochloride
Dosage FormTablet
RouteOral
Strengtheq 300mg base
Market StatusPrescription
CompanyGlaxo Grp

10 of 10  
Drug NameZantac 75
Drug LabelThe active ingredient in ZANTAC 150 Tablets, ZANTAC 300 Tablets, and ZANTAC Syrup is ranitidine hydrochloride (HCl), USP, a histamine H2-receptor antagonist. Chemically it is N[2-[[[5-[(dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]-N-methyl-2...
Active IngredientRanitidine hydrochloride
Dosage FormTablet
RouteOral
Strengtheq 75mg base
Market StatusOver the Counter
CompanyBoehringer Ingelheim

5 Pharmacology and Biochemistry
5.1 MeSH Pharmacological Classification

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.)


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.)


5.2 FDA Pharmacological Classification
5.2.1 Pharmacological Classes
Histamine-2 Receptor Antagonist [EPC]; Histamine H2 Receptor Antagonists [MoA]

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02-Jan-2021
08-Jan-2025
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DOSAGE - TABLET;ORAL - EQ 150MG BASE **Federa...DOSAGE - TABLET;ORAL - EQ 150MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

USFDA APPLICATION NUMBER - 18703

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DOSAGE - TABLET;ORAL - EQ 300MG BASE **Federa...DOSAGE - TABLET;ORAL - EQ 300MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

USFDA APPLICATION NUMBER - 18703

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DOSAGE - INJECTABLE;INJECTION - EQ 25MG BASE/...DOSAGE - INJECTABLE;INJECTION - EQ 25MG BASE/ML

USFDA APPLICATION NUMBER - 19090

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DOSAGE - TABLET;ORAL - EQ 75MG BASE

USFDA APPLICATION NUMBER - 20520

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DOSAGE - TABLET;ORAL - EQ 150MG BASE

USFDA APPLICATION NUMBER - 21698

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ABOUT THIS PAGE

Looking for 71130-06-8 / Ranitidine Hydrochloride API manufacturers, exporters & distributors?

Ranitidine Hydrochloride manufacturers, exporters & distributors 1

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PharmaCompass offers a list of Ranitidine Hydrochloride 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 Ranitidine Hydrochloride manufacturer or Ranitidine Hydrochloride supplier for your needs.

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

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

API | Excipient name

Ranitidine Hydrochloride

Synonyms

66357-59-3, 71130-06-8, Fendibina, Gastridina, Gastrolav, Kuracid

Cas Number

71130-06-8

About Ranitidine Hydrochloride

A non-imidazole blocker of those histamine receptors that mediate gastric secretion (H2 receptors). It is used to treat gastrointestinal ulcers.

Ranitidine HCL Manufacturers

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

Ranitidine HCL Suppliers

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

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

Ranitidine HCL USDMF

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

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

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

Ranitidine HCL 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 Ranitidine HCL Drug Master File in Japan (Ranitidine HCL JDMF) empowers Ranitidine HCL 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 Ranitidine HCL JDMF during the approval evaluation for pharmaceutical products. At the time of Ranitidine HCL 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 Ranitidine HCL suppliers with JDMF on PharmaCompass.

Ranitidine HCL KDMF

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

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

After submitting a Ranitidine HCL 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 Ranitidine HCL API can apply through the Korea Drug Master File (KDMF).

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

Ranitidine HCL CEP

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

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

Ranitidine HCL WC

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

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

Ranitidine HCL 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 Ranitidine HCL as an active pharmaceutical ingredient (API).

Finished drug products

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

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

Ranitidine HCL GMP

Ranitidine HCL 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 Ranitidine HCL 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 Ranitidine HCL GMP manufacturer or Ranitidine HCL GMP API supplier for your needs.

Ranitidine HCL CoA

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

Ranitidine HCL CoA mostly includes findings from lab analyses of a specific batch. For each Ranitidine HCL 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.

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