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Ranitidine
Zantac (ranitidine) is a small molecule pharmaceutical. Ranitidine was first approved as Zantac 150 on 1983-06-09. It is used to treat duodenal ulcer, gastroesophageal reflux, peptic esophagitis, stomach ulcer, and zollinger-ellison syndrome in the USA. The pharmaceutical is active against histamine H2 receptor.
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Commercial
Therapeutic Areas
Therapeutic Area
MeSH
neoplasmsD009369
digestive system diseasesD004066
Trade Name
FDA
EMA
No data
Drug Products
FDA
EMA
New Drug Application (NDA)
New Drug Application (NDA)
Abbreviated New Drug Application (ANDA)
Abbreviated New Drug Application (ANDA)
Ranitidine hydrochloride
Tradename
Company
Number
Date
Products
ZANTAC 75SanofiN-020520 DISCN1995-12-19
1 products, RLD
ZANTAC 75SanofiN-020745 DISCN1998-02-26
1 products, RLD
ZANTAC 150SanofiN-021698 DISCN2004-08-31
2 products, RLD
ZANTAC 300GSKN-018703 DISCN1985-12-09
1 products, RLD
ZANTAC 150GSKN-018703 DISCN1983-06-09
1 products, RLD
ZANTACGSKN-019675 DISCN1988-12-30
1 products, RLD
ZANTAC 25GSKN-020251 DISCN2004-04-01
1 products
ZANTAC 150GSKN-020251 DISCN1994-03-31
2 products
ZANTAC 150GSKN-020095 DISCN1994-03-08
1 products, RLD
ZANTAC 300GSKN-020095 DISCN1994-03-08
1 products, RLD
ZANTACPAI PharmaN-019090 DISCN1984-10-19
1 products, RLD
ZANTAC IN PLASTIC CONTAINERPAI PharmaN-019593 DISCN1986-12-17
2 products
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Labels
FDA
EMA
Brand Name
Status
Last Update
ranitidineANDA2023-01-27
zantac 360 cool mintANDA2022-12-01
Indications
FDA
EMA
Indication
Ontology
MeSH
ICD-10
duodenal ulcerEFO_0004607D004381K26
gastroesophageal refluxEFO_0003948D005764K21
peptic esophagitisEFO_1001095D004942—
stomach ulcer—D013276K25
zollinger-ellison syndrome—D015043E16.4
Agency Specific
FDA
EMA
No data
Patent Expiration
No data
ATC Codes
A: Alimentary tract and metabolism drugs
— A02: Drugs for acid related disorders
— A02B: Drugs for peptic ulcer and gastro-oesophageal reflux disease (gord)
— A02BA: H2-receptor antagonists
— A02BA02: Ranitidine
— A02BA07: Ranitidine bismuth citrate
HCPCS
Code
Description
J2780
Injection, ranitidine hydrochloride, 25 mg
Clinical
Clinical Trials
60 clinical trials
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Indications Phases 4
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
NeoplasmsD009369C8011—1—3
DyspepsiaD004415EFO_0008533K30———213
Drug-related side effects and adverse reactionsD064420T88.71——1—2
Coronary artery diseaseD003324I25.1———2—2
Drug interactionsD0043471——1—2
Prostatic neoplasmsD011471C61———1—1
VomitingD014839HP_0002013R11.1———1—1
NauseaD009325HP_0002018R11.0———1—1
Postoperative painD010149G89.18———1—1
Intestinal pseudo-obstructionD007418EFO_1000988K56.0———1—1
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Indications Phases 3
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Gastroesophageal refluxD005764EFO_0003948K21—13—15
Stomach ulcerD013276K25——3——3
Breast neoplasmsD001943EFO_0003869C50—21——2
Multiple sclerosisD009103EFO_0003885G35——1——1
CoughD003371HP_0012735R05——1——1
Indications Phases 2
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Hiv infectionsD015658EFO_0000764B2011———2
Immune system diseasesD007154D89.911———1
Renal cell carcinomaD002292—1———1
Postpartum hemorrhageD006473O72—1———1
Job syndromeD007589EFO_0003775D82.4—1———1
Renal insufficiencyD051437HP_0000083N19—1———1
Multiple myelomaD009101C90.0—1———1
Hematologic diseasesD006402EFO_0005803D75.9—1———1
Blood protein disordersD001796—1———1
Plasma cell neoplasmsD054219—1———1
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Indications Phases 1
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Healthy volunteers/patients—8————8
PharmacokineticsD0105993———14
Heart failureD006333EFO_0003144I501————1
HypertensionD006973EFO_0000537I101————1
Chronic obstructive pulmonary diseaseD029424EFO_0000341J44.91————1
Pulmonary arterial hypertensionD0000810291————1
Pure autonomic failureD0549701————1
Orthostatic hypotensionD007024I95.11————1
Hematologic neoplasmsD0193371————1
Precursor cell lymphoblastic leukemia-lymphomaD054198C91.01————1
Show 7 more
Indications Without Phase
Indication
MeSH
Ontology
ICD-10
Ph 1
Ph 2
Ph 3
Ph 4
Other
Total
Respiratory soundsD012135HP_0010307R06.1————11
LaryngomalaciaD055092HP_0001601————11
PoisoningD011041EFO_0008546T65.91————11
StrokeD020521EFO_0000712I63.9————11
Gastrointestinal diseasesD005767————11
Postoperative nausea and vomitingD020250EFO_0004888————11
Epidemiology
Epidemiological information for investigational and approved indications
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Drug
General
Drug common nameRANITIDINE
INNranitidine
Description
Ranitidine is a member of the class of furans used to treat peptic ulcer disease (PUD) and gastroesophageal reflux disease. It has a role as an anti-ulcer drug, a H2-receptor antagonist, an environmental contaminant, a xenobiotic and a drug allergen. It is a member of furans, a tertiary amino compound, a C-nitro compound and an organic sulfide.
Classification
Small molecule
Drug classH2-receptor antagonists (cimetidine type)
Image (chem structure or protein)
Structure (InChI/SMILES or Protein Sequence)
CNC(=C[N+](=O)[O-])NCCSCc1ccc(CN(C)C)o1
Identifiers
PDB—
CAS-ID66357-35-5
RxCUI—
ChEMBL IDCHEMBL1790041
ChEBI ID—
PubChem CID3001055
DrugBankDB00863
UNII ID884KT10YB7 (ChemIDplus, GSRS)
Target
Agency Approved
HRH2
HRH2
Organism
Homo sapiens
Gene name
HRH2
Gene synonyms
NCBI Gene ID
Protein name
histamine H2 receptor
Protein synonyms
gastric receptor 1, Gastric receptor I
Uniprot ID
Mouse ortholog
Hrh2 (15466)
histamine H2 receptor (Q9D282)
Alternate
No data
Variants
Clinical Variant
No data
Financial
Ranitidine - Amneal Pharmaceuticals
$
€
£
₣
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Tabular view
Trends
PubMed Central
Top Terms for Disease or Syndrome:
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Additional graphs summarizing 11,981 documents
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Safety
Black-box Warning
No Black-box warning
Adverse Events
Top Adverse Reactions
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510 adverse events reported
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