# acid controller

NDC: 37808-301
Generic name: Famotidine
Labeler / Manufacturer: H E B
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20151023

FDA application: ANDA075400

## Active ingredients

- FAMOTIDINE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"37808-301"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=37808-301
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=813d742f-8f3d-4f18-a6c5-03eea946f976