Dapagliflozin And Metformin Hydrochloride 63304-0027
Product NDC
63304-0027- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 6, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA211491
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Dapagliflozin | 10 mg/1 |
| Metformin Hydrochloride | 500 mg/1 |
Drug Class
Sodium-Glucose Cotransporter 2 Inhibitor [EPC]Biguanide [EPC]Biguanides [CS]
Packaging Options(2)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-027-30)
400 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63304-027-54)