# RANITIDINE HYDROCHLORIDE
> **ANDA077405** · Abbreviated New Drug Application (Generic) · Sponsor: PHARM ASSOC · Approved 2007-09-21
## Drug
- **FDA Application Number:** ANDA077405
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** RANITIDINE HYDROCHLORIDE
- **Generic name:** RANITIDINE
- **Active ingredients:** RANITIDINE HYDROCHLORIDE
- **Dosage form:** SYRUP
- **Route:** ORAL
- **Marketing status:** Discontinued
- **Sponsor:** PHARM ASSOC
- **Manufacturer:** Pharmaceutical Associates, Inc.
- **First approval:** 2007-09-21
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=077405)
---
*AI Analytics · CC0 1.0*