Zyclara - 29336-710-28 - (imiquimod)

Alphabetical Index


Drug Information of Zyclara

Product NDC: 29336-710
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: 29336-710
Labeler Name: Graceway Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022483
Marketing Category: NDA
Start Marketing Date: 20110815

Package Information of Zyclara

Package NDC: 29336-710-28
Package Description: 28 PACKET in 1 CARTON (29336-710-28) > 250 mg in 1 PACKET

NDC Information of Zyclara

NDC Code 29336-710-28
Proprietary Name Zyclara
Package Description 28 PACKET in 1 CARTON (29336-710-28) > 250 mg in 1 PACKET
Product NDC 29336-710
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name imiquimod
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20110815
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