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Ketorolac Tromethamine - 41616-221-90 - (Ketorolac Tromethamine)

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Drug Information of Ketorolac Tromethamine

Product NDC: 41616-221
Proprietary Name: Ketorolac Tromethamine
Non Proprietary Name: Ketorolac Tromethamine
Active Ingredient(s): 5    mg/mL & nbsp;   Ketorolac Tromethamine
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ketorolac Tromethamine

Product NDC: 41616-221
Labeler Name: Sun Pharma Global Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090017
Marketing Category: ANDA
Start Marketing Date: 20091106

Package Information of Ketorolac Tromethamine

Package NDC: 41616-221-90
Package Description: 10 mL in 1 BOTTLE (41616-221-90)

NDC Information of Ketorolac Tromethamine

NDC Code 41616-221-90
Proprietary Name Ketorolac Tromethamine
Package Description 10 mL in 1 BOTTLE (41616-221-90)
Product NDC 41616-221
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Ketorolac Tromethamine
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20091106
Marketing Category Name ANDA
Labeler Name Sun Pharma Global Inc.
Substance Name KETOROLAC TROMETHAMINE
Strength Number 5
Strength Unit mg/mL
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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