Vexol - 0065-0627-07 - (rimexolone)

Alphabetical Index


Drug Information of Vexol

Product NDC: 0065-0627
Proprietary Name: Vexol
Non Proprietary Name: rimexolone
Active Ingredient(s): 10    mg/mL & nbsp;   rimexolone
Administration Route(s): OPHTHALMIC
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Vexol

Product NDC: 0065-0627
Labeler Name: Alcon Laboratories, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020474
Marketing Category: NDA
Start Marketing Date: 19950915

Package Information of Vexol

Package NDC: 0065-0627-07
Package Description: 5 mL in 1 BOTTLE, PLASTIC (0065-0627-07)

NDC Information of Vexol

NDC Code 0065-0627-07
Proprietary Name Vexol
Package Description 5 mL in 1 BOTTLE, PLASTIC (0065-0627-07)
Product NDC 0065-0627
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name rimexolone
Dosage Form Name SUSPENSION
Route Name OPHTHALMIC
Start Marketing Date 19950915
Marketing Category Name NDA
Labeler Name Alcon Laboratories, Inc
Substance Name RIMEXOLONE
Strength Number 10
Strength Unit mg/mL
Pharmaceutical Classes Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA]

Complete Information of Vexol


General Information