NDC 59651-157 – Dapagliflozin and Metformin hydrochloride
Dapagliflozin 10 mg/1; Metformin Hydrochloride 1000 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC59651-157
Product details
- Brand name
- Dapagliflozin and Metformin hydrochloride
- Generic name
- Dapagliflozin and Metformin hydrochloride
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA211489
- Marketed since
- April 6, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Biguanide; Sodium-Glucose Cotransporter 2 Inhibitor
Active ingredients
- Dapagliflozin 10 mg/1
- Metformin Hydrochloride 1000 mg/1
Uses, dosage, side effects and warnings for dapagliflozin and metformin hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 59651-157-04 | 400 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-157-04) | Apr 6, 2026 |
| 59651-157-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59651-157-30) | Apr 6, 2026 |
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