NDC 80425-0591 – Metformin Hydrochloride
Metformin Hydrochloride 1000 mg/1 · Tablet, Film Coated · Oral
Product NDC80425-0591
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin hydrochloride
- Labeler
- Advanced Rx of Tennessee, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA075973
- Marketed since
- July 10, 2026
- Listing expires
- December 31, 2027
- Pharmacologic class
- Biguanide
Active ingredients
- Metformin Hydrochloride 1000 mg/1
Uses, dosage, side effects and warnings for Metformin hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 80425-0591-1 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0591-1) | Jul 10, 2026 |
| 80425-0591-2 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0591-2) | Jul 10, 2026 |
| 80425-0591-3 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0591-3) | Jul 10, 2026 |
| 80425-0591-4 | 108 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80425-0591-4) | Jul 10, 2026 |
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