metoprolol succinate
- Product NDC
- 53002-2612
- 11-digit product format
- 530022612
- Labeler code
- 53002
- Product ID
- 53002-2612_e3e35f97-6cb5-4b1c-a345-b9e941d53280
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metoprolol succinate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- Application
- ANDA204161
- Marketing category
- ANDA
- Marketing start
- 2020-02-03
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 53002-2612-0 | 53002261200 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53002-2612-0) | 2021-12-31 | 0000-00-00 | No | No | Current |
| 53002-2612-3 | 53002261203 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (53002-2612-3) | 2021-12-31 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| metoprolol succinate | RPK Pharmaceuticals, Inc. | 2022-04-20 | HUMAN PRESCRIPTION DRUG LABEL | 2 |