METOPROLOL TARTRATE
- Product NDC
- 70518-3950
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- METOPROLOL TARTRATE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA200981
- Marketing category
- ANDA
- Substance
- METOPROLOL TARTRATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 70518-3950-0 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3950-0) | 2023-12-11 | | No | Historical |
| 70518-3950-1 | 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3950-1) | 2023-12-25 | | No | Historical |
| 70518-3950-2 | 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3950-2) | 2024-07-11 | | No | Historical |
| 70518-3950-3 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3950-3) | 2025-07-31 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| METOPROLOL TARTRATE | REMEDYREPACK INC. | 2025-08-04 | HUMAN PRESCRIPTION DRUG LABEL | 5 |