NDC 60687-968 – Voriconazole

Voriconazole 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC60687-968

Product details

Brand name
Voriconazole
Generic name
Voriconazole
Labeler
American Health Packaging
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206837
Marketed since
August 27, 2026
Listing expires
December 31, 2027
Pharmacologic class
Azole Antifungal

Active ingredients

Uses, dosage, side effects and warnings for Voriconazole →

Package NDC codes (1)

Package NDCDescriptionSince
60687-968-2130 BLISTER PACK in 1 CARTON (60687-968-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-968-11)Aug 27, 2026

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