Metoprolol succinate
- Product NDC
- 72789-284
- 11-digit product format
- 727890284
- Labeler code
- 72789
- Product ID
- 72789-284_40bacd3a-ed47-93c6-e063-6294a90af100
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol succinate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA090617
- Marketing category
- ANDA
- Marketing start
- 2012-09-10
- 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 |
|---|
| 72789-284-30 | 72789028430 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-284-30) | 2022-10-25 | No | No | Historical |
| 72789-284-90 | 72789028490 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-284-90) | 2024-01-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Metoprolol succinate | PD-Rx Pharmaceuticals, Inc. | 2025-10-09 | HUMAN PRESCRIPTION DRUG LABEL | 13 |
| Metoprolol succinate | PD-Rx Pharmaceuticals, Inc. | 2024-01-11 | HUMAN PRESCRIPTION DRUG LABEL | 12 |