NDC 67877-591 – Metoprolol Succinate
Metoprolol Succinate 50 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC67877-591
Product details
- Brand name
- Metoprolol Succinate
- Generic name
- Metoprolol Succinate ER Tablets
- Labeler
- Ascend Laboratories, LLC
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA211143
- Marketed since
- November 27, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Metoprolol Succinate 50 mg/1
Uses, dosage, side effects and warnings for Metoprolol Succinate →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 67877-591-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-591-01) | Nov 27, 2020 |
| 67877-591-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-591-05) | Nov 27, 2020 |
| 67877-591-10 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-591-10) | Nov 27, 2020 |
| 67877-591-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-591-30) | Nov 27, 2020 |
| 67877-591-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (67877-591-60) | Nov 27, 2020 |
Recalls mentioning this NDC
- D-0547-2026 May 20, 2026 · Class II
Failed Dissolution Specifications - D-0170-2023 Feb 1, 2023 · Class II
Failed Dissolution Specification - D-0171-2023 Feb 1, 2023 · Class II
Failed Dissolution Specification - D-0169-2023 Feb 1, 2023 · Class II
Failed Dissolution Specification - D-0393-2022 Feb 2, 2022 · Class II
Failed Dissolution Specifications.
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