Zyclara - 29336-750-75 - (imiquimod)

Alphabetical Index


Drug Information of Zyclara

Product NDC: 29336-750
Proprietary Name: Zyclara
Non Proprietary Name: imiquimod
Active Ingredient(s): 3.75    mg/100mg & nbsp;   imiquimod
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Zyclara

Product NDC: 29336-750
Labeler Name: Graceway Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022483
Marketing Category: NDA
Start Marketing Date: 20111015

Package Information of Zyclara

Package NDC: 29336-750-75
Package Description: 7500 mg in 1 BOTTLE, PUMP (29336-750-75)

NDC Information of Zyclara

NDC Code 29336-750-75
Proprietary Name Zyclara
Package Description 7500 mg in 1 BOTTLE, PUMP (29336-750-75)
Product NDC 29336-750
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name imiquimod
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20111015
Marketing Category Name NDA
Labeler Name Graceway Pharmaceuticals, LLC
Substance Name IMIQUIMOD
Strength Number 3.75
Strength Unit mg/100mg
Pharmaceutical Classes Increased Cytokine Activity [PE],Increased Cytokine Production [PE],Interferon Inducers [MoA]

Complete Information of Zyclara


General Information