# RANITIDINE HYDROCHLORIDE
> **ANDA209859** · Abbreviated New Drug Application (Generic) · Sponsor: AJANTA PHARMA LTD · Approved 2018-09-27
## Drug
- **FDA Application Number:** 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
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=209859)
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