← FDA Drug Approvals (Drugs@FDA)
RANITIDINE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: GLENMARK PHARMS · Approved 2008-11-19
Drug application
- FDA Application #
ANDA078542- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- RANITIDINE HYDROCHLORIDE
- Generic name
- Ranitidine Hydrochloride
- Active ingredients
- RANITIDINE HYDROCHLORIDE
- Dosage form
- TABLET
- Route
- ORAL
- Marketing status
- Discontinued
- Sponsor
- GLENMARK PHARMS
- First approval
- 2008-11-19
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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