# Metformin Hydrochloride

NDC: 71205-884
Generic name: METFORMIN HYDROCHLORIDE
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20171121

FDA application: ANDA203769

## Active ingredients

- METFORMIN HYDROCHLORIDE: 1000 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-884"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-884
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=738402d6-3700-46b2-a90c-2e8f2c354a39