# Famotidine

NDC: 70756-052
Generic name: Famotidine
Labeler / Manufacturer: Lifestar Pharma LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20231019

FDA application: ANDA075302

## Active ingredients

- FAMOTIDINE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70756-052"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70756-052
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=044a510f-33df-4484-8f07-d821f52b9376