# Acid Reducer Maximum Strength

NDC: 43598-960
Generic name: Famotidine
Labeler / Manufacturer: Dr.Reddys Laboratories Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20200901

FDA application: ANDA077367

## 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:"43598-960"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-960
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ca039876-f7e5-3e60-da5a-a1f40637a417