NDC 33342-408 – Dapagliflozin and Metformin Hydrochloride
Dapagliflozin 5 mg/1; Metformin Hydrochloride 1000 mg/1 · Tablet, Extended Release · Oral
Product NDC33342-408
Product details
- Brand name
- Dapagliflozin and Metformin Hydrochloride
- Generic name
- Dapagliflozin and Metformin Hydrochloride
- Labeler
- Macleods Pharmaceuticals Limited
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA211559
- Marketed since
- April 6, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Biguanide; Sodium-Glucose Cotransporter 2 Inhibitor
Active ingredients
- Dapagliflozin 5 mg/1
- Metformin Hydrochloride 1000 mg/1
Uses, dosage, side effects and warnings for Dapagliflozin and metformin hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 33342-408-06 | 3 BLISTER PACK in 1 CARTON (33342-408-06) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (33342-408-66) | Apr 6, 2026 |
| 33342-408-07 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-408-07) | Apr 6, 2026 |
| 33342-408-09 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-408-09) | Apr 6, 2026 |
| 33342-408-10 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-408-10) | Apr 6, 2026 |
| 33342-408-15 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (33342-408-15) | Apr 6, 2026 |
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