NDC 68382-759 – Metformin Hydrochloride
Metformin Hydrochloride 850 mg/1 · Tablet, Film Coated · Oral
Product NDC68382-759
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin Hydrochloride
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA203686
- Marketed since
- December 9, 2014
- Listing expires
- December 31, 2027
- Pharmacologic class
- Biguanide
Active ingredients
- Metformin Hydrochloride 850 mg/1
Uses, dosage, side effects and warnings for Metformin hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 68382-759-01 | 100 TABLET, FILM COATED in 1 BOTTLE (68382-759-01) | Dec 9, 2014 |
| 68382-759-05 | 500 TABLET, FILM COATED in 1 BOTTLE (68382-759-05) | Dec 9, 2014 |
| 68382-759-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (68382-759-10) | Dec 9, 2014 |
| 68382-759-16 | 90 TABLET, FILM COATED in 1 BOTTLE (68382-759-16) | Dec 9, 2014 |
| 68382-759-77 | 100 BLISTER PACK in 1 CARTON (68382-759-77) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68382-759-30) | Dec 9, 2014 |
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