# Metformin Hydrochloride

NDC: 71610-578
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: 20181027

FDA application: ANDA206145

## Active ingredients

- METFORMIN HYDROCHLORIDE: 500 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71610-578"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71610-578
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1e298db3-439e-4e91-8f9e-01c3cdc4d552