Voriconazole

Product NDC

16714-515

11-digit product format

167140515

Labeler code

16714

Product ID

16714-515_59f0eb14-de52-4d6c-b555-31ef71cd7cca

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Voriconazole

Dosage form

TABLET

Route

ORAL

Labeler

Northstar Rx LLC

Application

ANDA206181

Marketing category

ANDA

Marketing start

2016-07-04

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

2021-12-31

Current FDA listing

Historical FDA.report record