METOPROLOL TARTRATE
- Product NDC
- 50090-7740
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METOPROLOL TARTRATE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA200981
- Marketing category
- ANDA
- Substance
- METOPROLOL TARTRATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-7740-0 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-7740-0) | 2025-10-29 | | No | Historical |
| 50090-7740-1 | 60 TABLET, FILM COATED in 1 BOTTLE (50090-7740-1) | 2025-10-29 | | No | Historical |
| 50090-7740-3 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-7740-3) | 2025-10-29 | | No | Historical |
| 50090-7740-4 | 180 TABLET, FILM COATED in 1 BOTTLE (50090-7740-4) | 2025-10-29 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| METOPROLOL TARTRATE | A-S Medication Solutions | 2025-11-02 | HUMAN PRESCRIPTION DRUG LABEL | 1 |