NDC 71335-3052 – Metoprolol Succinate
Metoprolol Succinate 50 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC71335-3052
Product details
- Brand name
- Metoprolol Succinate
- Generic name
- Metoprolol Succinate
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA216916
- Marketed since
- October 2, 2023
- 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 (7)
| Package NDC | Description | Since |
|---|---|---|
| 71335-3052-1 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3052-1) | May 21, 2026 |
| 71335-3052-2 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3052-2) | May 21, 2026 |
| 71335-3052-3 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3052-3) | May 21, 2026 |
| 71335-3052-4 | 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3052-4) | May 21, 2026 |
| 71335-3052-5 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3052-5) | May 21, 2026 |
| 71335-3052-6 | 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3052-6) | May 21, 2026 |
| 71335-3052-7 | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-3052-7) | May 21, 2026 |
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