# Metformin Hydrochloride

NDC: 70882-125
Generic name: Metformin Hydrochloride
Labeler / Manufacturer: Cambridge Therapeutics Technologies, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20110131

FDA application: ANDA091184

## Active ingredients

- METFORMIN HYDROCHLORIDE: 850 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70882-125"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70882-125
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c333ae3-a4df-483b-9103-762134add15e