Voriconazole 00781-5667
Product NDC
00781-5667- Manufacturer
- Sandoz Inc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 12, 2011
- Listing Expires
- December 31, 2027
- Application
- ANDA200265
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Voriconazole | 50 mg/1 |
Drug Class
Azole Antifungal [EPC]Azole Antifungal [EPC]Azoles [CS]
Packaging Options(4)
500 TABLET, FILM COATED in 1 BOTTLE (0781-5667-05)
1000 TABLET, FILM COATED in 1 BOTTLE (0781-5667-10)
10 BLISTER PACK in 1 CARTON (0781-5667-13) / 10 TABLET, FILM COATED in 1 BLISTER PACK (0781-5667-06)
30 TABLET, FILM COATED in 1 BOTTLE (0781-5667-31)