NDC 68462-572 – Voriconazole

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

Human Prescription Drug 2 recalls

Product NDC68462-572

Product details

Brand name
Voriconazole
Generic name
Voriconazole
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203503
Marketed since
September 4, 2015
Marketing end
November 1, 2026
Pharmacologic class
Azole Antifungal

Active ingredients

Uses, dosage, side effects and warnings for Voriconazole →

Package NDC codes (3)

Package NDCDescriptionSince
68462-572-133 BLISTER PACK in 1 CARTON (68462-572-13) / 10 TABLET, FILM COATED in 1 BLISTER PACKSep 4, 2015
68462-572-3030 TABLET, FILM COATED in 1 BOTTLE (68462-572-30)Sep 4, 2015
68462-572-9090 TABLET, FILM COATED in 1 BOTTLE (68462-572-90)Sep 4, 2015

Recalls mentioning this NDC

Other Voriconazole products