Ulesfia - 59630-780-08 - (benzyl alcohol)

Alphabetical Index


Drug Information of Ulesfia

Product NDC: 59630-780
Proprietary Name: Ulesfia
Non Proprietary Name: benzyl alcohol
Active Ingredient(s): 50    mg/g & nbsp;   benzyl alcohol
Administration Route(s): TOPICAL
Dosage Form(s): LOTION
Coding System: National Drug Codes(NDC)

Labeler Information of Ulesfia

Product NDC: 59630-780
Labeler Name: Shionogi Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022129
Marketing Category: NDA
Start Marketing Date: 20090526

Package Information of Ulesfia

Package NDC: 59630-780-08
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (59630-780-08) > 227 g in 1 BOTTLE, PLASTIC

NDC Information of Ulesfia

NDC Code 59630-780-08
Proprietary Name Ulesfia
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (59630-780-08) > 227 g in 1 BOTTLE, PLASTIC
Product NDC 59630-780
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name benzyl alcohol
Dosage Form Name LOTION
Route Name TOPICAL
Start Marketing Date 20090526
Marketing Category Name NDA
Labeler Name Shionogi Inc.
Substance Name BENZYL ALCOHOL
Strength Number 50
Strength Unit mg/g
Pharmaceutical Classes Pediculicide [EPC]

Complete Information of Ulesfia


General Information