# METFORMIN HYDROCHLORIDE

NDC: 71610-837
Generic name: metformin hydrochloride
Labeler / Manufacturer: Aphena Pharma Solutions - Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20130301

FDA application: ANDA201991

## Active ingredients

- METFORMIN HYDROCHLORIDE: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71610-837"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71610-837
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1a047fc0-196e-79af-e063-6394a90a1e0d