# acid relief

NDC: 11822-1014
Generic name: famotidine
Labeler / Manufacturer: Rite Aid Corporation
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220331

FDA application: ANDA077351

## 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:"11822-1014"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11822-1014
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=34034d16-dc3b-436d-8ec8-84b3c1f8e48a