← FDA Drug Approvals (Drugs@FDA)
RANITIDINE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: DR REDDYS LABS LTD · Approved 2000-11-29
Drug application
- FDA Application #
ANDA075742- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- RANITIDINE HYDROCHLORIDE
- Generic name
- RANITIDINE HYDROCHLORIDE
- Active ingredients
- RANITIDINE HYDROCHLORIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Marketing status
- Prescription
- Sponsor
- DR REDDYS LABS LTD
- Manufacturer
- Dr. Reddy's Laboratories Limited
- First approval
- 2000-11-29
Source
- Authoritative
- Drugs@FDA application overview
- Machine
- JSON-LD · Markdown