NDC 42571-334 – Metformin Hydrochloride
Metformin Hydrochloride 1000 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC42571-334
Product details
- Brand name
- Metformin Hydrochloride
- Generic name
- Metformin Hydrochloride
- Labeler
- Micro Labs Limited
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA212448
- Marketed since
- March 1, 2023
- Listing expires
- December 31, 2026
- Pharmacologic class
- Biguanide
Active ingredients
- Metformin Hydrochloride 1000 mg/1
Uses, dosage, side effects and warnings for Metformin hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 42571-334-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42571-334-01) | Mar 1, 2023 |
| 42571-334-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42571-334-05) | Mar 1, 2023 |
| 42571-334-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42571-334-60) | Mar 1, 2023 |
| 42571-334-90 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42571-334-90) | Mar 1, 2023 |
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