# FAMOTIDINE

NDC: 43602-602
Generic name: Famotidine
Labeler / Manufacturer: Ascent Pharmaceuticals, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20211103

FDA application: ANDA216030

## 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:"43602-602"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43602-602
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b481dd30-7d64-43ec-85d4-2289db62cad7