Zyclara - 99207-270-01 - (imiquimod)

Alphabetical Index


Drug Information of Zyclara

Product NDC: 99207-270
Proprietary Name: Zyclara
Non Proprietary Name: imiquimod
Active Ingredient(s): 37.5    mg/g & nbsp;   imiquimod
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Zyclara

Product NDC: 99207-270
Labeler Name: Medicis Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022483
Marketing Category: NDA
Start Marketing Date: 20111128

Package Information of Zyclara

Package NDC: 99207-270-01
Package Description: 4 PACKET in 1 CARTON (99207-270-01) > .25 g in 1 PACKET

NDC Information of Zyclara

NDC Code 99207-270-01
Proprietary Name Zyclara
Package Description 4 PACKET in 1 CARTON (99207-270-01) > .25 g in 1 PACKET
Product NDC 99207-270
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 37.5
Strength Unit mg/g
Pharmaceutical Classes Increased Cytokine Activity [PE],Increased Cytokine Production [PE],Interferon Inducers [MoA]

Complete Information of Zyclara


General Information