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KETOROLAC TROMETHAMINE - 49349-114-02 - (KETOROLAC TROMETHAMINE)

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Drug Information of KETOROLAC TROMETHAMINE

Product NDC: 49349-114
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
Coding System: National Drug Codes(NDC)

Labeler Information of KETOROLAC TROMETHAMINE

Product NDC: 49349-114
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074761
Marketing Category: ANDA
Start Marketing Date: 20101206

Package Information of KETOROLAC TROMETHAMINE

Package NDC: 49349-114-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-114-02)

NDC Information of KETOROLAC TROMETHAMINE

NDC Code 49349-114-02
Proprietary Name KETOROLAC TROMETHAMINE
Package Description 30 TABLET in 1 BLISTER PACK (49349-114-02)
Product NDC 49349-114
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name KETOROLAC TROMETHAMINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101206
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
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 TROMETHAMINE


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