TRUSOPT - 0006-3519-36 - (dorzolamide hydrochloride)

Alphabetical Index


Drug Information of TRUSOPT

Product NDC: 0006-3519
Proprietary Name: TRUSOPT
Non Proprietary Name: dorzolamide hydrochloride
Active Ingredient(s): 20    mg/mL & nbsp;   dorzolamide hydrochloride
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of TRUSOPT

Product NDC: 0006-3519
Labeler Name: Merck Sharp & Dohme Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020408
Marketing Category: NDA
Start Marketing Date: 19941209

Package Information of TRUSOPT

Package NDC: 0006-3519-36
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (0006-3519-36) > 10 mL in 1 BOTTLE, DROPPER

NDC Information of TRUSOPT

NDC Code 0006-3519-36
Proprietary Name TRUSOPT
Package Description 1 BOTTLE, DROPPER in 1 CARTON (0006-3519-36) > 10 mL in 1 BOTTLE, DROPPER
Product NDC 0006-3519
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name dorzolamide hydrochloride
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 19941209
Marketing Category Name NDA
Labeler Name Merck Sharp & Dohme Corp.
Substance Name DORZOLAMIDE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA]

Complete Information of TRUSOPT


General Information