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Ketorolac Tromethamine - 52959-512-12 - (Ketorolac Tromethamine)

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Drug Information of Ketorolac Tromethamine

Product NDC: 52959-512
Proprietary Name: Ketorolac Tromethamine
Non Proprietary Name: Ketorolac Tromethamine
Active Ingredient(s): 10    mg/1 & nbsp;   Ketorolac Tromethamine
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Ketorolac Tromethamine

Product NDC: 52959-512
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074754
Marketing Category: ANDA
Start Marketing Date: 20100420

Package Information of Ketorolac Tromethamine

Package NDC: 52959-512-12
Package Description: 12 TABLET, FILM COATED in 1 BOTTLE (52959-512-12)

NDC Information of Ketorolac Tromethamine

NDC Code 52959-512-12
Proprietary Name Ketorolac Tromethamine
Package Description 12 TABLET, FILM COATED in 1 BOTTLE (52959-512-12)
Product NDC 52959-512
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ketorolac Tromethamine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100420
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name KETOROLAC TROMETHAMINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ketorolac Tromethamine


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