Metoprolol Tartrate 57237-0102
Product NDC
57237-0102- Manufacturer
- Rising Pharma Holdings, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 11, 2007
- Listing Expires
- December 31, 2026
- Application
- ANDA077739
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Metoprolol Tartrate | 100 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(2)
100 TABLET, FILM COATED in 1 BOTTLE (57237-102-01)
1000 TABLET, FILM COATED in 1 BOTTLE (57237-102-99)