NDC 71335-2593 – Metformin Hydrochloride
Metformin Hydrochloride 850 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-2593
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA209882
- Marketed since
- May 17, 2021
- 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 (6)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2593-1 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2593-1) | Jun 4, 2025 |
| 71335-2593-2 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2593-2) | Jun 4, 2025 |
| 71335-2593-3 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-2593-3) | Jun 4, 2025 |
| 71335-2593-4 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-2593-4) | Jun 4, 2025 |
| 71335-2593-5 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-2593-5) | Jun 4, 2025 |
| 71335-2593-6 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-2593-6) | Jun 4, 2025 |
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