# Famotidine

NDC: 61442-121
Generic name: Famotidine
Labeler / Manufacturer: Carlsbad Technology, Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20010416

FDA application: ANDA075805

## 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:"61442-121"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=61442-121
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a8b5c855-053d-4295-8f57-1a96a6ccaa92