# FAMOTIDINE

NDC: 67877-842
Generic name: FAMOTIDINE
Labeler / Manufacturer: Ascend Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220708

FDA application: ANDA215630

## Active ingredients

- FAMOTIDINE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67877-842"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67877-842
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=be69d9f9-f4ad-4cfe-bab2-e07186b25c1e