NDC 63304-026-30
Dapagliflozin and Metformin Hydrochloride 5 mg/1
Dapagliflozin and Metformin Hydrochloride · TABLET, FILM COATED, EXTENDED RELEASE
Dapagliflozin and Metformin Hydrochloride is a tablet, film coated, extended release containing dapagliflozin and metformin hydrochloride at a strength of 5 mg/1. Manufactured by Sun Pharmaceutical Industries, Inc..
Key Facts
- Brand Name
- Dapagliflozin and Metformin Hydrochloride
- Generic Name
- Dapagliflozin and Metformin Hydrochloride
- NDC Code (Package)
63304-026-30- NDC Code (Product)
63304-026- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Strength
- 5 mg/1
- Dosage Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA211491
- Drug Class
- Sodium-Glucose Cotransporter 2 Inhibitor [EPC]
- Marketing Start
- 04/06/2026
Recall History
No Recall HistoryView Full Drug Page
Dapagliflozin and Metformin Hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.