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Ketorolac Tromethamine - 68788-9205-3 - (Ketorolac Tromethamine)

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Drug Information of Ketorolac Tromethamine

Product NDC: 68788-9205
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: 68788-9205
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074754
Marketing Category: ANDA
Start Marketing Date: 20100420

Package Information of Ketorolac Tromethamine

Package NDC: 68788-9205-3
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (68788-9205-3)

NDC Information of Ketorolac Tromethamine

NDC Code 68788-9205-3
Proprietary Name Ketorolac Tromethamine
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (68788-9205-3)
Product NDC 68788-9205
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 Preferred Pharmaceuticals, 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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