NDC 71335-3166 – Metformin Hydrochloride
Metformin Hydrochloride 500 mg/1 · Tablet, Extended Release · Oral
Product NDC71335-3166
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078321
- Marketed since
- February 15, 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 (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-3166-1 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3166-1) | Aug 4, 2026 |
| 71335-3166-2 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3166-2) | Aug 4, 2026 |
| 71335-3166-3 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3166-3) | Aug 4, 2026 |
| 71335-3166-4 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3166-4) | Aug 4, 2026 |
| 71335-3166-5 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3166-5) | Aug 4, 2026 |
| 71335-3166-6 | 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3166-6) | Aug 4, 2026 |
| 71335-3166-7 | 45 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3166-7) | Aug 4, 2026 |
| 71335-3166-8 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3166-8) | Aug 4, 2026 |
| 71335-3166-9 | 20 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-3166-9) | Aug 4, 2026 |
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