NDC 68001-501 – Metoprolol Succinate
Metoprolol Succinate 50 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC68001-501
Product details
- Brand name
- Metoprolol Succinate
- Generic name
- Metoprolol Succinate ER Tablets
- Labeler
- BluePoint Laboratories
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA211143
- Marketed since
- May 14, 2021
- Listing expires
- December 31, 2027
- Pharmacologic class
- beta-Adrenergic Blocker
Active ingredients
- Metoprolol Succinate 50 mg/1
Uses, dosage, side effects and warnings for Metoprolol Succinate →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68001-501-00 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-501-00) | May 14, 2021 |
| 68001-501-03 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68001-501-03) | May 14, 2021 |
Recalls mentioning this NDC
- D-0269-2023 Feb 22, 2023 · Class II
Failed Dissolution Specifications: This recall is being initiated in support of the recall by the manufacturer which included lots that were packaged for BluePoint Laboratories. - D-0451-2022 Feb 2, 2022 · Class II
Failed Dissolution Specifications
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