Carvedilol 68071-3138
Product NDC
68071-3138- Manufacturer
- Nucare Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 5, 2007
- Listing Expires
- December 31, 2026
- Application
- ANDA077614
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Carvedilol | 3.125 mg/1 |
Drug Class
alpha-Adrenergic Blocker [EPC]beta-Adrenergic Blocker [EPC]Adrenergic alpha-Antagonists [MoA]
Packaging Options(4)
30 TABLET, FILM COATED in 1 BOTTLE (68071-3138-3)
60 TABLET, FILM COATED in 1 BOTTLE (68071-3138-6)
180 TABLET, FILM COATED in 1 BOTTLE (68071-3138-8)
90 TABLET, FILM COATED in 1 BOTTLE (68071-3138-9)