NDC 45963-709 – Metoprolol succinate
Metoprolol Succinate 25 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC45963-709
Product details
- Brand name
- Metoprolol succinate
- Generic name
- Metoprolol succinate
- Labeler
- Actavis Pharma, Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA204161
- Marketed since
- October 23, 2019
- Marketing end
- August 31, 2027
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Metoprolol Succinate 25 mg/1
Uses, dosage, side effects and warnings for Metoprolol Succinate →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 45963-709-11 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45963-709-11) | Oct 23, 2019 |
| 45963-709-96 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45963-709-96) | Oct 23, 2019 |
Recalls mentioning this NDC
- D-0355-2026 Mar 11, 2026 · Class II
Failed Dissolution Specifications - D-0357-2026 Mar 11, 2026 · Class II
Failed Dissolution Specifications - D-0354-2026 Mar 11, 2026 · Class II
Failed Dissolution Specifications - D-0356-2026 Mar 11, 2026 · Class II
Failed Dissolution Specifications - D-0191-2024 Jan 3, 2024 · Class II
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
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- 45963-677 Metoprolol Succinate 100 mg/1 · Tablet, Film Coated, Extended Release · Actavis Pharma, Inc.
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