FDA
Ranitidine Hydrochloride
The FDA lists this product in 60 strengths and forms.
Composition
- Active ingredients
- RANITIDINE HYDROCHLORIDE EQ 75MG BASE
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- RANITIDINE HYDROCHLORIDE EQ 15MG BASE/ML · SyrupANDA079212-001 · Discontinued
- RANITIDINE HYDROCHLORIDE EQ 300MG BASE · CapsuleANDA210681-002 · Discontinued
- RANITIDINE HYDROCHLORIDE EQ 150MG BASE · CapsuleANDA210681-001 · Discontinued
- RANITIDINE HYDROCHLORIDE EQ 150MG BASE · TabletANDA074662-001 · Discontinued
- RANITIDINE HYDROCHLORIDE EQ 300MG BASE · TabletANDA074662-002 · Discontinued
- RANITIDINE HYDROCHLORIDE EQ 25MG BASE/ML · InjectableANDA074764-001 · Discontinued
- RANITIDINE HYDROCHLORIDE EQ 150MG BASE · TabletANDA074864-001 · Discontinued
- RANITIDINE HYDROCHLORIDE EQ 300MG BASE · TabletANDA074864-002 · Discontinued
- RANITIDINE HYDROCHLORIDE EQ 75MG BASE · TabletANDA075254-001 · Discontinued
- RANITIDINE HYDROCHLORIDE EQ 75MG BASE · TabletANDA076195-001 · Discontinued
- RANITIDINE HYDROCHLORIDE EQ 300MG BASE · Tablet
At a glance
- Brand name
- Ranitidine Hydrochloride
- Route
- Oral
- Dosage form
- Tablet
- Applicant
- Wockhardt
- Status
- Discontinued
- FDA approval
- 31 Jul 2008
- Application
- ANDA078884-001