Metoprolol Succinate
- Product NDC
- 72162-1856
- 11-digit product format
- 721621856
- Labeler code
- 72162
- Product ID
- 72162-1856_99dbab93-287f-4e75-9a7c-003b90c7449c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Succinate ER Tablets
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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 |
|---|
| 72162-1856-0 | 72162185600 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1856-0) | 2024-03-05 | No | No | Historical |
| 72162-1856-1 | 72162185601 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1856-1) | 2024-03-05 | No | No | Historical |
| 72162-1856-5 | 72162185605 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72162-1856-5) | 2024-03-05 | No | No | Historical |