Metoprolol Succinate
- Product NDC
- 68788-8869
- 11-digit product format
- 687888869
- Labeler code
- 68788
- Product ID
- 68788-8869_21e18c1c-fabb-44a4-a33a-b02a47967d73
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA216916
- Marketing category
- ANDA
- Marketing start
- 2025-04-30
- 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 |
|---|
| 68788-8869-3 | 68788886903 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8869-3) | 2025-04-30 | No | No | Historical |
| 68788-8869-6 | 68788886906 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8869-6) | 2025-04-30 | No | No | Historical |
| 68788-8869-9 | 68788886909 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-8869-9) | 2025-04-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Metoprolol Succinate | Preferred Pharmaceuticals Inc. | 2025-04-30 | HUMAN PRESCRIPTION DRUG LABEL | 1 |