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Ketotifen Fumarate - 17478-717-11 - (Ketotifen Fumarate)

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Drug Information of Ketotifen Fumarate

Product NDC: 17478-717
Proprietary Name: Ketotifen Fumarate
Non Proprietary Name: Ketotifen Fumarate
Active Ingredient(s): .35    mg/mL & nbsp;   Ketotifen Fumarate
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Ketotifen Fumarate

Product NDC: 17478-717
Labeler Name: Akorn, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077958
Marketing Category: ANDA
Start Marketing Date: 20071001

Package Information of Ketotifen Fumarate

Package NDC: 17478-717-11
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (17478-717-11) > 10 mL in 1 BOTTLE, DROPPER

NDC Information of Ketotifen Fumarate

NDC Code 17478-717-11
Proprietary Name Ketotifen Fumarate
Package Description 1 BOTTLE, DROPPER in 1 CARTON (17478-717-11) > 10 mL in 1 BOTTLE, DROPPER
Product NDC 17478-717
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ketotifen Fumarate
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20071001
Marketing Category Name ANDA
Labeler Name Akorn, Inc.
Substance Name KETOTIFEN FUMARATE
Strength Number .35
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Ketotifen Fumarate


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