Metoprolol Tartrate
- Product NDC
- 71872-7283
- 11-digit product format
- 718727283
- Labeler code
- 71872
- Product ID
- 71872-7283_fab7143c-d976-94a9-e053-6394a90a060c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA204205
- Marketing category
- ANDA
- Marketing start
- 2019-03-18
- Substance
- METOPROLOL TARTRATE
- Active strength
- 5 mg/5mL
- Pharmacologic classes
- Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| W5S57Y3A5L | METOPROLOL TARTRATE | 56392-17-7 | METOPROLOL TARTRATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7283-1 | 71872728301 | 1 VIAL, SINGLE-DOSE in 1 BAG (71872-7283-1) / 5 mL in 1 VIAL, SINGLE-DOSE | 2022-03-11 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Metoprolol Tartrate | Medical Purchasing Solutions, LLC | 2023-05-02 | HUMAN PRESCRIPTION DRUG LABEL | 2 |