NDC 71335-0776 – Metformin Hydrochloride
Metformin Hydrochloride 750 mg/1 · Tablet, Extended Release · Oral
Product NDC71335-0776
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078321
- Marketed since
- April 17, 2008
- Listing expires
- December 31, 2026
- Pharmacologic class
- Biguanide
Active ingredients
- Metformin Hydrochloride 750 mg/1
Uses, dosage, side effects and warnings for Metformin hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0776-1 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0776-1) | Apr 17, 2018 |
| 71335-0776-2 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0776-2) | Apr 17, 2018 |
| 71335-0776-3 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0776-3) | Apr 17, 2018 |
| 71335-0776-4 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0776-4) | Apr 17, 2018 |
| 71335-0776-5 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0776-5) | Apr 17, 2018 |
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