NDC product
Dapagliflozin and Metformin Hydrochloride
NDC 63304-026 · Sun Pharmaceutical Industries, Inc.
Key facts
| Product NDC | 63304-026 |
|---|---|
| Proprietary name | Dapagliflozin and Metformin Hydrochloride |
| Nonproprietary name | Dapagliflozin and Metformin Hydrochloride |
| Substances | DAPAGLIFLOZIN, METFORMIN HYDROCHLORIDE |
| Dosage form | TABLET, FILM COATED, EXTENDED RELEASE |
| Route | ORAL |
| Labeler | Sun Pharmaceutical Industries, Inc. |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Application number | ANDA211491 |
| Pharmacologic classes | Biguanide [EPC], Biguanides [CS], Sodium-Glucose Cotransporter 2 Inhibitor [EPC], Sodium-Glucose Transporter 2 Inhibitors [MoA] |
| Marketing start | Apr 6, 2026 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: