# FAMOTIDINE
> **ANDA218631** · Abbreviated New Drug Application (Generic) · Sponsor: REGCON HOLDINGS · Approved 2025-03-25
## Drug
- **FDA Application Number:** ANDA218631
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** FAMOTIDINE
- **Generic name:** Famotidine
- **Active ingredients:** FAMOTIDINE
- **Dosage form:** TABLET
- **Route:** ORAL
- **Marketing status:** Prescription
- **Sponsor:** REGCON HOLDINGS
- **First approval:** 2025-03-25
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=218631)
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