Metoprolol Tartrate
- Product NDC
- 71872-7225
- 11-digit product format
- 718727225
- Labeler code
- 71872
- Product ID
- 71872-7225_fae66e91-be0b-9128-e053-6394a90ac25d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Metoprolol Tartrate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- ANDA077761
- Marketing category
- ANDA
- Marketing start
- 2007-05-30
- 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7225-1 | 71872722501 | 1 VIAL in 1 BAG (71872-7225-1) / 5 mL in 1 VIAL | 1 vial | 2020-11-30 | No | No | Historical |