NDC 70710-2036 – Sitagliptin and Metformin Hydrochloride
Sitagliptin 50 mg/1; Metformin Hydrochloride 500 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC70710-2036
Product details
- Brand name
- Sitagliptin and Metformin Hydrochloride
- Generic name
- Sitagliptin and metformin hydrochloride
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA216778
- Marketed since
- October 31, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Biguanide; Dipeptidyl Peptidase 4 Inhibitor
Active ingredients
- Sitagliptin 50 mg/1
- Metformin Hydrochloride 500 mg/1
Uses, dosage, side effects and warnings for Sitagliptin and Metformin Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 70710-2036-6 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-2036-6) | Oct 31, 2024 |
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