NDC 65841-830 – Voriconazole

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

Human Prescription Drug

Product NDC65841-830

Product details

Brand name
Voriconazole
Generic name
Voriconazole
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA206747
Marketed since
May 25, 2016
Listing expires
December 31, 2027
Pharmacologic class
Azole Antifungal

Active ingredients

Uses, dosage, side effects and warnings for Voriconazole →

Package NDC codes (6)

Package NDCDescriptionSince
65841-830-01100 TABLET, FILM COATED in 1 BOTTLE (65841-830-01)May 25, 2016
65841-830-05500 TABLET, FILM COATED in 1 BOTTLE (65841-830-05)May 25, 2016
65841-830-0630 TABLET, FILM COATED in 1 BOTTLE (65841-830-06)May 25, 2016
65841-830-101000 TABLET, FILM COATED in 1 BOTTLE (65841-830-10)May 25, 2016
65841-830-1690 TABLET, FILM COATED in 1 BOTTLE (65841-830-16)May 25, 2016
65841-830-7710 BLISTER PACK in 1 CARTON (65841-830-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65841-830-30)May 25, 2016

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