Istalol - 24208-004-03 - (Timolol Maleate)

Alphabetical Index


Drug Information of Istalol

Product NDC: 24208-004
Proprietary Name: Istalol
Non Proprietary Name: Timolol Maleate
Active Ingredient(s): 6.8    mg/mL & nbsp;   Timolol Maleate
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Istalol

Product NDC: 24208-004
Labeler Name: Bausch & Lomb Incorporated
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021516
Marketing Category: NDA
Start Marketing Date: 20040802

Package Information of Istalol

Package NDC: 24208-004-03
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (24208-004-03) > 5 mL in 1 BOTTLE, DROPPER

NDC Information of Istalol

NDC Code 24208-004-03
Proprietary Name Istalol
Package Description 1 BOTTLE, DROPPER in 1 CARTON (24208-004-03) > 5 mL in 1 BOTTLE, DROPPER
Product NDC 24208-004
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Timolol Maleate
Dosage Form Name SOLUTION/ DROPS
Route Name OPHTHALMIC
Start Marketing Date 20040802
Marketing Category Name NDA
Labeler Name Bausch & Lomb Incorporated
Substance Name TIMOLOL MALEATE
Strength Number 6.8
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

Complete Information of Istalol


General Information