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eye itch relief - 59779-982-01 - (Ketotifen Fumarate)

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Drug Information of eye itch relief

Product NDC: 59779-982
Proprietary Name: eye itch relief
Non Proprietary Name: Ketotifen Fumarate
Active Ingredient(s): .25    g/mL & nbsp;   Ketotifen Fumarate
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of eye itch relief

Product NDC: 59779-982
Labeler Name: CVS Pharmacy
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077958
Marketing Category: ANDA
Start Marketing Date: 20100914

Package Information of eye itch relief

Package NDC: 59779-982-01
Package Description: 1 BOTTLE in 1 CARTON (59779-982-01) > 5 mL in 1 BOTTLE

NDC Information of eye itch relief

NDC Code 59779-982-01
Proprietary Name eye itch relief
Package Description 1 BOTTLE in 1 CARTON (59779-982-01) > 5 mL in 1 BOTTLE
Product NDC 59779-982
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Ketotifen Fumarate
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 20100914
Marketing Category Name ANDA
Labeler Name CVS Pharmacy
Substance Name KETOTIFEN FUMARATE
Strength Number .25
Strength Unit g/mL
Pharmaceutical Classes

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