NDC 68788-4022 – Metoprolol Succinate
Metoprolol Succinate 25 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC68788-4022
Product details
- Brand name
- Metoprolol Succinate
- Generic name
- Metoprolol Succinate
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA216916
- Marketed since
- September 5, 2025
- 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 |
|---|---|---|
| 68788-4022-3 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-4022-3) | Sep 5, 2025 |
| 68788-4022-6 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-4022-6) | Sep 5, 2025 |
| 68788-4022-9 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-4022-9) | Sep 5, 2025 |
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