NDC 59651-855 – Metformin Hydrochloride
Metformin Hydrochloride 850 mg/1 · Tablet, Film Coated · Oral
Product NDC59651-855
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin Hydrochloride
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077095
- Marketed since
- March 29, 2024
- Listing expires
- December 31, 2027
- Pharmacologic class
- Biguanide
Active ingredients
- Metformin Hydrochloride 850 mg/1
Uses, dosage, side effects and warnings for Metformin hydrochloride →
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 59651-855-01 | 100 TABLET, FILM COATED in 1 BOTTLE (59651-855-01) | Mar 29, 2024 |
| 59651-855-05 | 500 TABLET, FILM COATED in 1 BOTTLE (59651-855-05) | Mar 29, 2024 |
| 59651-855-26 | 2500 TABLET, FILM COATED in 1 BOTTLE (59651-855-26) | Mar 29, 2024 |
| 59651-855-50 | 50 TABLET, FILM COATED in 1 BOTTLE (59651-855-50) | Mar 29, 2024 |
| 59651-855-60 | 60 TABLET, FILM COATED in 1 BOTTLE (59651-855-60) | Mar 29, 2024 |
| 59651-855-79 | 300 TABLET, FILM COATED in 1 BOTTLE (59651-855-79) | Mar 29, 2024 |
| 59651-855-90 | 90 TABLET, FILM COATED in 1 BOTTLE (59651-855-90) | Mar 29, 2024 |
| 59651-855-99 | 1000 TABLET, FILM COATED in 1 BOTTLE (59651-855-99) | Mar 29, 2024 |
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