# Dapagliflozin and Metformin Hydrochloride

NDC: 63304-028
Generic name: Dapagliflozin and Metformin Hydrochloride
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED, EXTENDED RELEASE
Routes: ORAL
Marketing started: 20260406

FDA application: ANDA211491

## Active ingredients

- DAPAGLIFLOZIN: 10 mg/1
- METFORMIN HYDROCHLORIDE: 1000 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63304-028"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63304-028
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bddc2d47-8d3d-4c2f-8e5c-7a1a0782219a