# FAMOTIDINE

NDC: 68788-8485
Generic name: FAMOTIDINE
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230718

FDA application: ANDA215630

## Active ingredients

- FAMOTIDINE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68788-8485"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8485
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b445a613-eaa8-45e8-be1f-5848bfd1dd36