Metoprolol Tartrate
- Product NDC
- 50090-7362
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA077739
- Marketing category
- ANDA
- Substance
- METOPROLOL TARTRATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-7362-0 | 180 TABLET, FILM COATED in 1 BOTTLE (50090-7362-0) | 2024-10-18 | | No | Historical |
| 50090-7362-1 | 60 TABLET, FILM COATED in 1 BOTTLE (50090-7362-1) | 2024-10-18 | | No | Historical |
| 50090-7362-2 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-7362-2) | 2024-10-18 | | No | Historical |
| 50090-7362-3 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-7362-3) | 2024-10-18 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Metoprolol Tartrate | A-S Medication Solutions | 2024-10-22 | Human Prescription Drug Label | 21 |