42291-442 NDC - IBUPROFEN ()

Drug Information

Product NDC: 42291-442

Proprietary Name: Ibuprofen

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Pharmacy Class(es):

No.	Package Code	Package Description	Billing Unit
1	42291-442-30	30 TABLET, FILM COATED in 1 BOTTLE (42291-442-30)	EA
2	42291-442-90	90 TABLET, FILM COATED in 1 BOTTLE (42291-442-90)	EA
3	42291-442-95	500 TABLET, FILM COATED in 1 BOTTLE (42291-442-95)

Field Name	Field Value	Definition
PRODUCT NDC	42291-442	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	Ibuprofen	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	6/1/2021	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	AvKARE	Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC	42291-442	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	Ibuprofen	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	9/3/2020	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	AvKARE	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