Xalatan - 0013-8303-04 - (LATANOPROST)

Alphabetical Index


Drug Information of Xalatan

Product NDC: 0013-8303
Proprietary Name: Xalatan
Non Proprietary Name: LATANOPROST
Active Ingredient(s): 50    ug/mL & nbsp;   LATANOPROST
Administration Route(s): OPHTHALMIC
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Xalatan

Product NDC: 0013-8303
Labeler Name: Pharmacia and Upjohn Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020597
Marketing Category: NDA
Start Marketing Date: 19950320

Package Information of Xalatan

Package NDC: 0013-8303-04
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (0013-8303-04) > 2.5 mL in 1 BOTTLE, DROPPER

NDC Information of Xalatan

NDC Code 0013-8303-04
Proprietary Name Xalatan
Package Description 1 BOTTLE, DROPPER in 1 CARTON (0013-8303-04) > 2.5 mL in 1 BOTTLE, DROPPER
Product NDC 0013-8303
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name LATANOPROST
Dosage Form Name SOLUTION
Route Name OPHTHALMIC
Start Marketing Date 19950320
Marketing Category Name NDA
Labeler Name Pharmacia and Upjohn Company
Substance Name LATANOPROST
Strength Number 50
Strength Unit ug/mL
Pharmaceutical Classes Prostaglandin Analog [EPC],Prostaglandins [Chemical/Ingredient]

Complete Information of Xalatan


General Information