metoprolol succinate
- Product NDC
- 51655-934
- 11-digit product format
- 516550934
- Labeler code
- 51655
- Product ID
- 51655-934_4bbd9310-c072-86ae-e063-6294a90a92ee
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metoprolol succinate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Northwind Health Company, LLC
- Application
- ANDA204161
- Marketing category
- ANDA
- Marketing start
- 2022-07-25
- Substance
- METOPROLOL SUCCINATE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- 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 |
|---|
| 51655-934-26 | 51655093426 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-934-26) | 2022-07-25 | No | No | Historical |
| 51655-934-52 | 51655093452 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-934-52) | 2022-09-16 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| metoprolol succinate | Northwind Health Company, LLC | 2026-01-01 | HUMAN PRESCRIPTION DRUG LABEL | 5 |