Voriconazole

Product NDC

42291-900

11-digit product format

422910900

Labeler code

42291

Product ID

42291-900_641af79f-51e2-6fd3-e053-2991aa0ad158

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Voriconazole

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

AvKARE, Inc.

Application

ANDA091658

Marketing category

ANDA

Marketing start

2016-02-25

Marketing end

0000-00-00

Substance

VORICONAZOLE

Active strength

200 mg/1

Pharmacologic classes

Azole Antifungal [EPC],Azoles [CS],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA],Cytochrome P450 2C9 Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record