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Ketorolac Tromethamine - 55154-8264-0 - (Ketorolac Tromethamine)

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Drug Information of Ketorolac Tromethamine

Product NDC: 55154-8264
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: 55154-8264
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074754
Marketing Category: ANDA
Start Marketing Date: 20100420

Package Information of Ketorolac Tromethamine

Package NDC: 55154-8264-0
Package Description: 10 POUCH in 1 BAG (55154-8264-0) > 1 TABLET, FILM COATED in 1 POUCH

NDC Information of Ketorolac Tromethamine

NDC Code 55154-8264-0
Proprietary Name Ketorolac Tromethamine
Package Description 10 POUCH in 1 BAG (55154-8264-0) > 1 TABLET, FILM COATED in 1 POUCH
Product NDC 55154-8264
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 Cardinal Health
Substance Name KETOROLAC TROMETHAMINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ketorolac Tromethamine


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