← FDA Drug Approvals (Drugs@FDA)
RANITIDINE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: AJANTA PHARMA LTD · Approved 2018-09-27
Drug application
- FDA Application #
ANDA209859- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- RANITIDINE HYDROCHLORIDE
- Generic name
- RANITIDINE
- Active ingredients
- RANITIDINE HYDROCHLORIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Marketing status
- Discontinued
- Sponsor
- AJANTA PHARMA LTD
- Manufacturer
- Ajanta Pharma USA Inc.
- First approval
- 2018-09-27
Source
- Authoritative
- Drugs@FDA application overview
- Machine
- JSON-LD · Markdown