Metoprolol Tartrate
- Product NDC
- 50090-7363
- 11-digit product format
- 500907363
- Labeler code
- 50090
- Product ID
- 50090-7363_c4ee814e-352b-4f8b-8aa0-c7084b3ab6b8
- 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
- Marketing start
- 2007-09-11
- Substance
- METOPROLOL TARTRATE
- Active strength
- 25 mg/1
- 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 |
|---|
| 50090-7363-0 | 50090736300 | 90 TABLET, FILM COATED in 1 BOTTLE (50090-7363-0) | 2024-10-18 | No | 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 |