61715-053 NDC - PREFERRED PLUS IBUPROFEN 200 ()

Drug Information

Product NDC: 61715-053

Proprietary Name: Preferred Plus Ibuprofen 200

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Kinray
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/26/2013

Package Information

No. Package Code Package Description Billing Unit
161715-053-011 TABLET in 1 CARTON (61715-053-01)
261715-053-088 TABLET in 1 BLISTER PACK (61715-053-08)

NDC Record

Field Name Field Value Definition
PRODUCT NDC61715-053The 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 NAMEPreferred Plus Ibuprofen 200The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/26/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEKinrayName 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