Details for New Drug Application (NDA): 211482
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The generic ingredient in DAPAGLIFLOZIN is dapagliflozin; saxagliptin hydrochloride. There are twenty-six drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the dapagliflozin; saxagliptin hydrochloride profile page.
Summary for 211482
| Tradename: | DAPAGLIFLOZIN |
| Applicant: | Ajanta Pharma Ltd |
| Ingredient: | dapagliflozin |
| Patents: | 0 |
Pharmacology for NDA: 211482
| Mechanism of Action | Sodium-Glucose Transporter 2 Inhibitors |
Suppliers and Packaging for NDA: 211482
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| DAPAGLIFLOZIN | dapagliflozin | TABLET;ORAL | 211482 | ANDA | Ajanta Pharma USA Inc. | 27241-151 | 27241-151-01 | 30 TABLET in 1 BOTTLE (27241-151-01) |
| DAPAGLIFLOZIN | dapagliflozin | TABLET;ORAL | 211482 | ANDA | Ajanta Pharma USA Inc. | 27241-152 | 27241-152-01 | 30 TABLET in 1 BOTTLE (27241-152-01) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 5MG | ||||
| Approval Date: | Apr 6, 2026 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | 10MG | ||||
| Approval Date: | Apr 6, 2026 | TE: | AB | RLD: | No | ||||
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