59726-199 NDC - IBUPROFEN ()

Drug Information

Product NDC: 59726-199

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:1/29/2021

Package Information

No. Package Code Package Description Billing Unit
159726-199-101 BOTTLE, PLASTIC in 1 BOX (59726-199-10) / 10 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC
259726-199-16160 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC (59726-199-16)
359726-199-201 BOTTLE, PLASTIC in 1 BOX (59726-199-20) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC

NDC Record

Field Name Field Value Definition
PRODUCT NDC59726-199The 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 DATE1/29/2021This 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