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Ketorolac Tromethamine - 49349-737-40 - (KETOROLAC TROMETHAMINE)

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Drug Information of Ketorolac Tromethamine

Product NDC: 49349-737
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: 49349-737
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074754
Marketing Category: ANDA
Start Marketing Date: 20120904

Package Information of Ketorolac Tromethamine

Package NDC: 49349-737-40
Package Description: 25 TABLET in 1 BLISTER PACK (49349-737-40)

NDC Information of Ketorolac Tromethamine

NDC Code 49349-737-40
Proprietary Name Ketorolac Tromethamine
Package Description 25 TABLET in 1 BLISTER PACK (49349-737-40)
Product NDC 49349-737
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name KETOROLAC TROMETHAMINE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120904
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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