KETOROLAC - 16590-138-30 - (KETOROLAC TROMETHAMINE)

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Drug Information of KETOROLAC

Product NDC: 16590-138
Proprietary Name: KETOROLAC
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

Product NDC: 16590-138
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074761
Marketing Category: ANDA
Start Marketing Date: 20100915

Package Information of KETOROLAC

Package NDC: 16590-138-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (16590-138-30)

NDC Information of KETOROLAC

NDC Code 16590-138-30
Proprietary Name KETOROLAC
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (16590-138-30)
Product NDC 16590-138
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name KETOROLAC TROMETHAMINE
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100915
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
Substance Name KETOROLAC TROMETHAMINE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of KETOROLAC


General Information