# Metformin Hydrochloride

NDC: 72336-064
Generic name: Metformin Hydrochloride
Labeler / Manufacturer: Lifsa Drugs, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20020124

FDA application: ANDA075972

## Active ingredients

- METFORMIN HYDROCHLORIDE: 625 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72336-064"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72336-064
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a2385bcd-0943-4411-8658-c22b50360385