Home > National Drug Code (NDC) > Lotrimin Ultra

Lotrimin Ultra - 11523-7154-2 - (Butenafine Hydrochloride)

Alphabetical Index


Drug Information of Lotrimin Ultra

Product NDC: 11523-7154
Proprietary Name: Lotrimin Ultra
Non Proprietary Name: Butenafine Hydrochloride
Active Ingredient(s): 10    mg/g & nbsp;   Butenafine Hydrochloride
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Lotrimin Ultra

Product NDC: 11523-7154
Labeler Name: MSD Consumer Care, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: NDA021307
Marketing Category: NDA
Start Marketing Date: 19930923

Package Information of Lotrimin Ultra

Package NDC: 11523-7154-2
Package Description: 1 TUBE in 1 CARTON (11523-7154-2) > 24 g in 1 TUBE

NDC Information of Lotrimin Ultra

NDC Code 11523-7154-2
Proprietary Name Lotrimin Ultra
Package Description 1 TUBE in 1 CARTON (11523-7154-2) > 24 g in 1 TUBE
Product NDC 11523-7154
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Butenafine Hydrochloride
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 19930923
Marketing Category Name NDA
Labeler Name MSD Consumer Care, Inc.
Substance Name BUTENAFINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/g
Pharmaceutical Classes

Complete Information of Lotrimin Ultra


General Information