# Metformin Hydrochloride

NDC: 0615-8015
Generic name: Metformin Hydrochloride
Labeler / Manufacturer: NCS HealthCare of KY, LLC dba Vangard Labs
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20050114
Marketing ended: 20270131
FDA application: ANDA077095

## 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:"0615-8015"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0615-8015
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=23aa0072-365c-4d13-9aa7-ae23f7e00ee4