52959-512 NDC - KETOROLAC TROMETHAMINE ()

Drug Information

Product NDC: 52959-512

Proprietary Name: Ketorolac Tromethamine

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: H.J. Harkins Company, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/20/2010

Package Information

No. Package Code Package Description Billing Unit
152959-512-088 TABLET, FILM COATED in 1 BOTTLE (52959-512-08)EA
252959-512-099 TABLET, FILM COATED in 1 BOTTLE (52959-512-09)EA
352959-512-1010 TABLET, FILM COATED in 1 BOTTLE (52959-512-10)EA
452959-512-1212 TABLET, FILM COATED in 1 BOTTLE (52959-512-12)EA
552959-512-1414 TABLET, FILM COATED in 1 BOTTLE (52959-512-14)EA
652959-512-1515 TABLET, FILM COATED in 1 BOTTLE (52959-512-15)EA
752959-512-2020 TABLET, FILM COATED in 1 BOTTLE (52959-512-20)EA
852959-512-3030 TABLET, FILM COATED in 1 BOTTLE (52959-512-30)EA
952959-512-4040 TABLET, FILM COATED in 1 BOTTLE (52959-512-40)EA
1052959-512-6060 TABLET, FILM COATED in 1 BOTTLE (52959-512-60)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC52959-512The 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 NAMEKetorolac TromethamineThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/20/2010This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEH.J. Harkins Company, Inc.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