# Metformin Hydrochloride

NDC: 71205-686
Generic name: Metformin Hydrochloride
Labeler / Manufacturer: Proficient Rx LP
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

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-686"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-686
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=474e2900-43bf-4ebe-9d29-4a7adb8a9429
