Metoprolol succinate
- Product NDC
- 68071-3828
- 11-digit product format
- 680713828
- Labeler code
- 68071
- Product ID
- 68071-3828_32340827-2dbb-dfe5-e063-6294a90ab085
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol succinate
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceutcals, Inc.
- 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 |
|---|
| 68071-3828-1 | 68071382801 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3828-1) | 2025-04-07 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Metoprolol succinate | NuCare Pharmaceutcals, Inc. | 2025-04-07 | HUMAN PRESCRIPTION DRUG LABEL | 1 |