NDC 68788-7205 – Metformin Hydrochloride
Metformin Hydrochloride 750 mg/1 · Tablet, Extended Release · Oral
Product NDC68788-7205
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin Hydrochloride
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078321
- Marketed since
- July 23, 2018
- Marketing end
- September 30, 2026
- Pharmacologic class
- Biguanide
Active ingredients
- Metformin Hydrochloride 750 mg/1
Uses, dosage, side effects and warnings for Metformin hydrochloride →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 68788-7205-1 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7205-1) | Jul 23, 2018 |
| 68788-7205-3 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7205-3) | Jul 23, 2018 |
| 68788-7205-6 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7205-6) | Jul 23, 2018 |
| 68788-7205-8 | 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7205-8) | Jul 23, 2018 |
| 68788-7205-9 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7205-9) | Jul 23, 2018 |
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