NDC 71335-3132 – Metformin Hydrochloride
Metformin Hydrochloride 500 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-3132
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077095
- Marketed since
- March 29, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Biguanide
Active ingredients
- Metformin Hydrochloride 500 mg/1
Uses, dosage, side effects and warnings for Metformin hydrochloride →
Package NDC codes (10)
| Package NDC | Description | Since |
|---|---|---|
| 71335-3132-0 | 25 TABLET, FILM COATED in 1 BOTTLE (71335-3132-0) | Aug 26, 2026 |
| 71335-3132-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-3132-1) | Aug 3, 2026 |
| 71335-3132-2 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-3132-2) | Jul 6, 2026 |
| 71335-3132-3 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-3132-3) | Jul 22, 2026 |
| 71335-3132-4 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-3132-4) | Aug 26, 2026 |
| 71335-3132-5 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-3132-5) | May 12, 2026 |
| 71335-3132-6 | 28 TABLET, FILM COATED in 1 BOTTLE (71335-3132-6) | Aug 26, 2026 |
| 71335-3132-7 | 56 TABLET, FILM COATED in 1 BOTTLE (71335-3132-7) | Aug 26, 2026 |
| 71335-3132-8 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-3132-8) | Aug 26, 2026 |
| 71335-3132-9 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-3132-9) | Aug 26, 2026 |
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