Metoprolol Succinate
- Product NDC
- 71335-2945
- 11-digit product format
- 713352945
- Labeler code
- 71335
- Product ID
- 71335-2945_0c03da67-eb57-43db-a446-084c9fa0705c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA216916
- Marketing category
- ANDA
- Marketing start
- 2023-10-02
- Substance
- METOPROLOL SUCCINATE
- Active strength
- 100 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| TH25PD4CCB | METOPROLOL SUCCINATE | 98418-47-4 | METOPROLOL SUCCINATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2945-1 | 71335294501 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2945-1) | 2025-10-28 | No | No | Historical |
| 71335-2945-2 | 71335294502 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2945-2) | 2025-10-28 | No | No | Historical |
| 71335-2945-3 | 71335294503 | 120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2945-3) | 2025-10-28 | No | No | Historical |
| 71335-2945-4 | 71335294504 | 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2945-4) | 2025-10-28 | No | No | Historical |
| 71335-2945-5 | 71335294505 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2945-5) | 2025-10-28 | No | No | Historical |
| 71335-2945-6 | 71335294506 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2945-6) | 2025-10-28 | No | No | Historical |
| 71335-2945-7 | 71335294507 | 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-2945-7) | 2025-10-28 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Metoprolol Succinate | Bryant Ranch Prepack | 2025-10-28 | HUMAN PRESCRIPTION DRUG LABEL | 1 |