54162-540 NDC - KERATEK ()

Drug Information

Product NDC: 54162-540

Proprietary Name: KERATEK

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: GERITREX CORP
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/21/2013

Package Information

No. Package Code Package Description Billing Unit
154162-540-04113 g in 1 BOTTLE (54162-540-04)GM

NDC Record

Field Name Field Value Definition
PRODUCT NDC54162-540The 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 NAMEKERATEKThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/21/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEGERITREX CORPName 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