metoprolol succinate
- Product NDC
- 71205-801
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- metoprolol succinate
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA204161
- Marketing category
- ANDA
- Substance
- METOPROLOL SUCCINATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71205-801-30 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-801-30) | 2023-05-18 | | No | Historical |
| 71205-801-60 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-801-60) | 2023-05-18 | | No | Historical |
| 71205-801-90 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71205-801-90) | 2023-05-18 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| metoprolol succinate | Proficient Rx LP | 2023-05-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |