# Metformin Hydrochloride

NDC: 25000-131
Generic name: Metformin Hydrochloride
Labeler / Manufacturer: MARKSANS PHARMA LIMITED
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20120601

FDA application: ANDA090888

## Active ingredients

- METFORMIN HYDROCHLORIDE: 850 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"25000-131"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=25000-131
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b8004451-7b26-425b-b5ea-cbb1b08e30e3
