# Maximum Strength Acid Controller

NDC: 21130-027
Generic name: Famotidine
Labeler / Manufacturer: BETTER LIVING BRANDS LLC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230623

FDA application: ANDA217543

## 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:"21130-027"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=21130-027
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f2c031b4-de86-3a8e-e053-2a95a90a21e0