Carvedilol 00904-7305
Product NDC
00904-7305- Manufacturer
- Major Pharmaceuticals
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 1, 2024
- Listing Expires
- December 31, 2027
- Application
- ANDA078251
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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(1)
100 BLISTER PACK in 1 CARTON (0904-7305-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK