NDC 70010-780 – Metoprolol Succinate
Metoprolol Succinate 25 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC70010-780
Product details
- Brand name
- Metoprolol Succinate
- Generic name
- Metoprolol Succinate
- Labeler
- Granules Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA216916
- Marketed since
- October 2, 2023
- 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 (3)
| Package NDC | Description | Since |
|---|---|---|
| 70010-780-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-780-01) | Oct 2, 2023 |
| 70010-780-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-780-05) | Oct 2, 2023 |
| 70010-780-10 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70010-780-10) | Oct 2, 2023 |
Recalls mentioning this NDC
- D-0510-2025 Jul 9, 2025 · Class II
Failed Dissolution Specifications: Product failed to meet dissolution acceptance criteria in the stability studies at the 6th month (25¿C/60% RH) long-term.
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