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Ketorolac Tromethamine - 17478-209-19 - (ketorolac tromethamine)

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Drug Information of Ketorolac Tromethamine

Product NDC: 17478-209
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: 17478-209
Labeler Name: Akorn Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078434
Marketing Category: ANDA
Start Marketing Date: 20091105

Package Information of Ketorolac Tromethamine

Package NDC: 17478-209-19
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (17478-209-19) > 3 mL in 1 BOTTLE, DROPPER

NDC Information of Ketorolac Tromethamine

NDC Code 17478-209-19
Proprietary Name Ketorolac Tromethamine
Package Description 1 BOTTLE, DROPPER in 1 CARTON (17478-209-19) > 3 mL in 1 BOTTLE, DROPPER
Product NDC 17478-209
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ketorolac tromethamine
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20091105
Marketing Category Name ANDA
Labeler Name Akorn 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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