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Timolol GFS - 61314-224-25 - (timolol maleate)

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Drug Information of Timolol GFS

Product NDC: 61314-224
Proprietary Name: Timolol GFS
Non Proprietary Name: timolol maleate
Active Ingredient(s): 2.5    mg/mL & nbsp;   timolol maleate
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION, GEL FORMING, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Timolol GFS

Product NDC: 61314-224
Labeler Name: FALCON Pharmaceuticals, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020963
Marketing Category: NDA
Start Marketing Date: 19981224

Package Information of Timolol GFS

Package NDC: 61314-224-25
Package Description: 2.5 mL in 1 BOTTLE (61314-224-25)

NDC Information of Timolol GFS

NDC Code 61314-224-25
Proprietary Name Timolol GFS
Package Description 2.5 mL in 1 BOTTLE (61314-224-25)
Product NDC 61314-224
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name timolol maleate
Dosage Form Name SOLUTION, GEL FORMING, EXTENDED RELEASE
Route Name OPHTHALMIC
Start Marketing Date 19981224
Marketing Category Name NDA
Labeler Name FALCON Pharmaceuticals, Ltd.
Substance Name TIMOLOL MALEATE
Strength Number 2.5
Strength Unit mg/mL
Pharmaceutical Classes

Complete Information of Timolol GFS


General Information