NDC 68788-8756 – Metformin Hydrochloride
Metformin Hydrochloride 850 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-8756
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin Hydrochloride
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA209882
- Marketed since
- October 14, 2024
- 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 |
|---|---|---|
| 68788-8756-1 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-8756-1) | Oct 14, 2024 |
| 68788-8756-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8756-3) | Oct 14, 2024 |
| 68788-8756-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8756-6) | Oct 14, 2024 |
| 68788-8756-8 | 120 TABLET, FILM COATED in 1 BOTTLE (68788-8756-8) | Oct 14, 2024 |
| 68788-8756-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8756-9) | Oct 14, 2024 |
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