NDC 68462-520 – Metformin Hydrochloride
Metformin Hydrochloride 500 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC68462-520
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin hydrochloride
- Labeler
- GLENMARK PHARMACEUTICALS INC., USA
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA212969
- Marketed since
- November 25, 2019
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 68462-520-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-520-01) | Nov 25, 2019 |
| 68462-520-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-520-05) | Nov 25, 2019 |
| 68462-520-10 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-520-10) | Nov 25, 2019 |
Recalls mentioning this NDC
- D-0328-2025 Apr 16, 2025 · Class II
CGMP Deviations
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