# Metformin Hydrochloride

NDC: 51655-644
Generic name: Metformin Hydrochloride
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230706

FDA application: ANDA209882

## Active ingredients

- METFORMIN HYDROCHLORIDE: 1000 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-644"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-644
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0178b9dd-bafa-9e81-e063-6294a90a88b0