Imiquimod - 68462-536-70 - (Imiquimod)

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Drug Information of Imiquimod

Product NDC: 68462-536
Proprietary Name: Imiquimod
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 Imiquimod

Product NDC: 68462-536
Labeler Name: Glenmark Generics Inc.,USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201994
Marketing Category: ANDA
Start Marketing Date: 20120306

Package Information of Imiquimod

Package NDC: 68462-536-70
Package Description: 24 PACKET in 1 CARTON (68462-536-70) > .25 g in 1 PACKET

NDC Information of Imiquimod

NDC Code 68462-536-70
Proprietary Name Imiquimod
Package Description 24 PACKET in 1 CARTON (68462-536-70) > .25 g in 1 PACKET
Product NDC 68462-536
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Imiquimod
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20120306
Marketing Category Name ANDA
Labeler Name Glenmark Generics Inc.,USA
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 Imiquimod


General Information