Metoprolol Tartrate
- Product NDC
- 68071-5236
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA200981
- Marketing category
- ANDA
- Substance
- METOPROLOL TARTRATE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 68071-5236-1 | 100 TABLET, FILM COATED in 1 BOTTLE (68071-5236-1) | 2020-04-03 | Yes | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| METOPROLOL TARTRATE TABLETS, USP TruPharma LLC R x only | NuCare Pharmaceuticals,Inc. | 2024-06-20 | HUMAN PRESCRIPTION DRUG LABEL | 3 |