# Metformin Hydrochloride

NDC: 72578-036
Generic name: Metformin Hydrochloride
Labeler / Manufacturer: Viona Pharmaceuticals Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20190315

FDA application: ANDA077078

## Active ingredients

- METFORMIN HYDROCHLORIDE: 750 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72578-036"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72578-036
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=85027e6c-d35b-49eb-a234-dd71aa77aee0