# Famotidine

NDC: 83008-091
Generic name: Famotidine
Labeler / Manufacturer: Quality Care Products, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20240918
Marketing ended: 20261231
FDA application: ANDA075718

## 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:"83008-091"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83008-091
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3549386a-533d-4e44-8097-f6bc51ee494a