Voriconazole 00904-7024
Product NDC
00904-7024- Manufacturer
- Major Pharmaceuticals
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 31, 2016
- Listing Expires
- December 31, 2027
- Application
- ANDA206181
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Voriconazole | 200 mg/1 |
Drug Class
Azole Antifungal [EPC]Azole Antifungal [EPC]Azoles [CS]
Packaging Options(1)
30 BLISTER PACK in 1 CARTON (0904-7024-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK