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Ketorolac Tromethamine - 0093-0314-01 - (Ketorolac Tromethamine)

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Drug Information of Ketorolac Tromethamine

Product NDC: 0093-0314
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: 0093-0314
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074754
Marketing Category: ANDA
Start Marketing Date: 19980617

Package Information of Ketorolac Tromethamine

Package NDC: 0093-0314-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (0093-0314-01)

NDC Information of Ketorolac Tromethamine

NDC Code 0093-0314-01
Proprietary Name Ketorolac Tromethamine
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (0093-0314-01)
Product NDC 0093-0314
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ketorolac Tromethamine
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19980617
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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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