Metformin Hydrochloride 47335-0306
Product NDC
47335-0306- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 22, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA202917
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Metformin Hydrochloride | 1000 mg/1 |
Drug Class
Biguanide [EPC]Biguanides [CS]
Packaging Options(4)
1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-306-18)
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-306-81)
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-306-83)
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-306-88)