FDA
Cimetidine Hydrochloride
The FDA lists this product in 19 strengths and forms.
Composition
- Active ingredients
- CIMETIDINE HYDROCHLORIDE EQ 300MG BASE/5ML
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- CIMETIDINE HYDROCHLORIDE EQ 300MG BASE/5ML · SolutionANDA075110-001 · Discontinued
- CIMETIDINE HYDROCHLORIDE EQ 300MG BASE/2ML · InjectableANDA074353-001 · Discontinued
- CIMETIDINE HYDROCHLORIDE EQ 300MG BASE/2ML · InjectableANDA074428-001 · Discontinued
- CIMETIDINE HYDROCHLORIDE EQ 300MG BASE/5ML · SolutionANDA074664-001 · Prescription
- CIMETIDINE HYDROCHLORIDE EQ 300MG BASE/5ML · SolutionANDA074610-001 · Discontinued
- CIMETIDINE HYDROCHLORIDE EQ 300MG BASE/2ML · InjectableANDA074344-001 · Discontinued
- CIMETIDINE HYDROCHLORIDE EQ 300MG BASE/2ML · InjectableANDA074412-001 · Discontinued
- CIMETIDINE HYDROCHLORIDE EQ 300MG BASE/2ML · InjectableANDA074422-001 · Discontinued
- CIMETIDINE HYDROCHLORIDE EQ 300MG BASE/5ML · SolutionThis page
- CIMETIDINE HYDROCHLORIDE EQ 300MG BASE/5ML · SolutionANDA074757-001 · Discontinued
At a glance
- Brand name
- Cimetidine Hydrochloride
- Route
- Oral
- Dosage form
- Solution
- Applicant
- Pharm Assoc
- Status
- Discontinued
- FDA approval
- 27 Jan 1997
- Application
- ANDA074553-001