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RANITIDINE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: SUN PHARMA CANADA · Approved 2011-06-13
Drug application
- FDA Application #
ANDA077476- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- RANITIDINE HYDROCHLORIDE
- Generic name
- Ranitidine Hydrochloride
- Active ingredients
- RANITIDINE HYDROCHLORIDE
- Dosage form
- SYRUP
- Route
- ORAL
- Marketing status
- Discontinued
- Sponsor
- SUN PHARMA CANADA
- First approval
- 2011-06-13
Source
- Authoritative
- Drugs@FDA application overview
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