Metoprolol Tartrate 68071-4880
Product NDC
68071-4880- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 1, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA200981
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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)
120 TABLET, FILM COATED in 1 BOTTLE (68071-4880-1)
90 TABLET, FILM COATED in 1 BOTTLE (68071-4880-9)