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TIMOLOL MALEATE - 60758-802-10 - (timolol maleate)

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Drug Information of TIMOLOL MALEATE

Product NDC: 60758-802
Proprietary Name: TIMOLOL MALEATE
Non Proprietary Name: timolol maleate
Active Ingredient(s): 2.5    mg/mL & nbsp;   timolol maleate
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of TIMOLOL MALEATE

Product NDC: 60758-802
Labeler Name: Pacific Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074746
Marketing Category: ANDA
Start Marketing Date: 19970520

Package Information of TIMOLOL MALEATE

Package NDC: 60758-802-10
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (60758-802-10) > 10 mL in 1 BOTTLE, DROPPER

NDC Information of TIMOLOL MALEATE

NDC Code 60758-802-10
Proprietary Name TIMOLOL MALEATE
Package Description 1 BOTTLE, DROPPER in 1 CARTON (60758-802-10) > 10 mL in 1 BOTTLE, DROPPER
Product NDC 60758-802
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name timolol maleate
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 19970520
Marketing Category Name ANDA
Labeler Name Pacific Pharma, Inc.
Substance Name TIMOLOL MALEATE
Strength Number 2.5
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of TIMOLOL MALEATE


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