Aldara - 99207-260-12 - (imiquimod)

Alphabetical Index


Drug Information of Aldara

Product NDC: 99207-260
Proprietary Name: Aldara
Non Proprietary Name: imiquimod
Active Ingredient(s): 50    mg/g & nbsp;   imiquimod
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Aldara

Product NDC: 99207-260
Labeler Name: Medicis Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020723
Marketing Category: NDA
Start Marketing Date: 20111128

Package Information of Aldara

Package NDC: 99207-260-12
Package Description: 12 PACKET in 1 CARTON (99207-260-12) > .25 g in 1 PACKET

NDC Information of Aldara

NDC Code 99207-260-12
Proprietary Name Aldara
Package Description 12 PACKET in 1 CARTON (99207-260-12) > .25 g in 1 PACKET
Product NDC 99207-260
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name imiquimod
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20111128
Marketing Category Name NDA
Labeler Name Medicis Pharmaceutical Corp
Substance Name IMIQUIMOD
Strength Number 50
Strength Unit mg/g
Pharmaceutical Classes Increased Cytokine Activity [PE],Increased Cytokine Production [PE],Interferon Inducers [MoA]

Complete Information of Aldara


General Information