ILEVRO - 0065-1750-07 - (nepafenac)

Alphabetical Index


Drug Information of ILEVRO

Product NDC: 0065-1750
Proprietary Name: ILEVRO
Non Proprietary Name: nepafenac
Active Ingredient(s): 3    mg/mL & nbsp;   nepafenac
Administration Route(s): OPHTHALMIC
Dosage Form(s): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of ILEVRO

Product NDC: 0065-1750
Labeler Name: Alcon Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA203491
Marketing Category: NDA
Start Marketing Date: 20121220

Package Information of ILEVRO

Package NDC: 0065-1750-07
Package Description: 1 BOTTLE, DROPPER in 1 CARTON (0065-1750-07) > 1.7 mL in 1 BOTTLE, DROPPER

NDC Information of ILEVRO

NDC Code 0065-1750-07
Proprietary Name ILEVRO
Package Description 1 BOTTLE, DROPPER in 1 CARTON (0065-1750-07) > 1.7 mL in 1 BOTTLE, DROPPER
Product NDC 0065-1750
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name nepafenac
Dosage Form Name SUSPENSION
Route Name OPHTHALMIC
Start Marketing Date 20121220
Marketing Category Name NDA
Labeler Name Alcon Laboratories, Inc.
Substance Name NEPAFENAC
Strength Number 3
Strength Unit mg/mL
Pharmaceutical Classes Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC]

Complete Information of ILEVRO


General Information