# METFORMIN HYDROCHLORIDE

NDC: 68462-520
Generic name: metformin hydrochloride
Labeler / Manufacturer: GLENMARK PHARMACEUTICALS INC., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20191125

FDA application: ANDA212969

## 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:"68462-520"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-520
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0ef9de1a-b786-4b6c-a250-3f5ac532b16a