NDC 51655-649 – Metformin Hydrochloride
Metformin Hydrochloride 1000 mg/1 · Tablet, Film Coated · Oral
Product NDC51655-649
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin Hydrochloride
- Labeler
- Northwind Health Company, LLC
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077095
- Marketed since
- April 1, 2021
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 51655-649-25 | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-649-25) | Jul 23, 2025 |
| 51655-649-26 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-649-26) | Jun 23, 2023 |
| 51655-649-52 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-649-52) | Apr 1, 2021 |
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