| NDC Code | 72205-438-02 |
|---|
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (72205-438-02) |
|---|
| Product NDC | 72205-438 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Dapagliflozin And Saxagliptin |
|---|
| Non-Proprietary Name | Dapagliflozin And Saxagliptin |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20260406 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA211533 |
|---|
| Manufacturer | Novadoz Pharmaceuticals LLC |
|---|
| Substance Name | DAPAGLIFLOZIN; SAXAGLIPTIN HYDROCHLORIDE DIHYDRATE |
|---|
| Strength | 10; 5 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Sodium-Glucose Cotransporter 2 Inhibitor [EPC], Sodium-Glucose Transporter 2 Inhibitors [MoA] |
|---|