NDC 68788-8600 – Metformin Hydrochloride
Metformin Hydrochloride 1000 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-8600
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
- March 8, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Biguanide
Active ingredients
- Metformin Hydrochloride 1000 mg/1
Uses, dosage, side effects and warnings for Metformin hydrochloride →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 68788-8600-1 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-8600-1) | Mar 8, 2024 |
| 68788-8600-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-8600-3) | Mar 8, 2024 |
| 68788-8600-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-8600-6) | Mar 8, 2024 |
| 68788-8600-7 | 180 TABLET, FILM COATED in 1 BOTTLE (68788-8600-7) | Mar 8, 2024 |
| 68788-8600-8 | 120 TABLET, FILM COATED in 1 BOTTLE (68788-8600-8) | Mar 8, 2024 |
| 68788-8600-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-8600-9) | Mar 8, 2024 |
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