NDC 31722-589 – Metoprolol Succinate
Metoprolol Succinate 25 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC31722-589
Product details
- Brand name
- Metoprolol Succinate
- Generic name
- Metoprolol Succinate
- Labeler
- Camber Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA205541
- Marketed since
- November 6, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Metoprolol Succinate 25 mg/1
Uses, dosage, side effects and warnings for Metoprolol Succinate →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 31722-589-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-589-01) | Nov 6, 2020 |
| 31722-589-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-589-05) | Apr 23, 2021 |
| 31722-589-10 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-589-10) | Apr 23, 2021 |
| 31722-589-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-589-30) | Nov 6, 2020 |
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