Metoprolol Succinate
- Product NDC
- 82804-252
- 11-digit product format
- 828040252
- Labeler code
- 82804
- Product ID
- 82804-252_33d39ddc-478a-4d98-80d1-f655202192ae
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate ER Tablets
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA211143
- Marketing category
- ANDA
- Marketing start
- 2020-11-27
- 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
- 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 |
|---|
| 82804-252-90 | 82804025290 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (82804-252-90) | 2025-11-04 | No | No | Historical |