# CareOne Acid Relief

NDC: 41520-707
Generic name: Famotidine
Labeler / Manufacturer: American Sales Company
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20160922

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:"41520-707"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=41520-707
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=206f5483-7de1-4bc3-af27-190e211bcb95
