Dapagliflozin 59651-0159
Product NDC
59651-0159- Manufacturer
- Aurobindo Pharma Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 6, 2026
- Listing Expires
- December 31, 2027
- Application
- ANDA211468
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Dapagliflozin | 5 mg/1 |
Drug Class
Sodium-Glucose Cotransporter 2 Inhibitor [EPC]Sodium-Glucose Cotransporter 2 Inhibitor [EPC]Sodium-Glucose Transporter 2 Inhibitors [MoA]
Packaging Options(2)
30 TABLET, FILM COATED in 1 BOTTLE (59651-159-30)
90 TABLET, FILM COATED in 1 BOTTLE (59651-159-90)