# METFORMIN HYDROCHLORIDE

NDC: 71335-9683
Generic name: METFORMIN HYDROCHLORIDE
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20200806

FDA application: ANDA076756

## 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:"71335-9683"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-9683
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=86627ff4-da1c-429d-991b-88e97f6967d6