40032-089 NDC - VORICONAZOLE ()

Drug Information

Product NDC: 40032-089

Proprietary Name: voriconazole

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description
1	40032-089-03	30 TABLET, FILM COATED in 1 BOTTLE (40032-089-03)
2	40032-089-05	500 TABLET, FILM COATED in 1 BOTTLE (40032-089-05)
3	40032-089-31	3 BLISTER PACK in 1 CARTON (40032-089-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK (40032-089-30)

Field Name	Field Value	Definition
PRODUCT NDC	40032-089	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAME	voriconazole	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	5/24/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Novel Laboratories, Inc.	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023