NDC 51655-368 – Metformin Hydrochloride
Metformin Hydrochloride 750 mg/1 · Tablet, Extended Release · Oral
Product NDC51655-368
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin Hydrochloride
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA078321
- Marketed since
- June 4, 2020
- Marketing end
- November 30, 2026
- Pharmacologic class
- Biguanide
Active ingredients
- Metformin Hydrochloride 750 mg/1
Uses, dosage, side effects and warnings for Metformin hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 51655-368-52 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-368-52) | Jun 4, 2020 |
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