Metoprolol succinate
- Product NDC
- 50090-7239
- 11-digit product format
- 500907239
- Labeler code
- 50090
- Product ID
- 50090-7239_92658b35-7389-4451-a769-18ebb18e081c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol succinate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA090617
- Marketing category
- ANDA
- Marketing start
- 2023-04-10
- Substance
- METOPROLOL SUCCINATE
- Active strength
- 50 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 |
|---|
| 50090-7239-0 | 50090723900 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7239-0) | 2024-09-10 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Metoprolol succinate | A-S Medication Solutions | 2025-09-05 | HUMAN PRESCRIPTION DRUG LABEL | 5 |
| Metoprolol succinate | A-S Medication Solutions | 2024-09-12 | HUMAN PRESCRIPTION DRUG LABEL | 3 |