NDC 69238-2126 – Metformin Hydrochloride
Metformin Hydrochloride 750 mg/1 · Tablet, Extended Release · Oral
Product NDC69238-2126
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin Hydrochloride
- Labeler
- Amneal Pharmaceuticals LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078596
- Marketed since
- February 26, 2010
- Listing expires
- December 31, 2027
- Pharmacologic class
- Biguanide
Active ingredients
- Metformin Hydrochloride 750 mg/1
Uses, dosage, side effects and warnings for Metformin hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 69238-2126-1 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (69238-2126-1) | Feb 26, 2010 |
| 69238-2126-3 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69238-2126-3) | Feb 26, 2010 |
| 69238-2126-5 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (69238-2126-5) | Feb 26, 2010 |
| 69238-2126-9 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69238-2126-9) | Feb 26, 2010 |
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