# Maximum Strength Acid Reducer

NDC: 11673-697
Generic name: Famotidine
Labeler / Manufacturer: TARGET CORPORATION
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20240515

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:"11673-697"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11673-697
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=07a924f1-14cc-4e7d-e063-6394a90ac7f3