59726-661 NDC - IBUPROFEN ()

Drug Information

Product NDC: 59726-661

Proprietary Name: Ibuprofen

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: P & L Development, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/31/2017

Package Information

No. Package Code Package Description Billing Unit
159726-661-401 BOTTLE, PLASTIC in 1 BOX (59726-661-40) / 40 TABLET, COATED in 1 BOTTLE, PLASTIC
259726-661-501 BOTTLE, PLASTIC in 1 BOX (59726-661-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC

NDC Record

Field Name Field Value Definition
PRODUCT NDC59726-661The 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 NAMEIbuprofenThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/31/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEP & L Development, LLCName 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