Drug Master Files for: imiquimod

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imiquimod Drug Master Files

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DMF No.	Status	Type	Submission Date	Holder	Subject
18031	A	II	1/26/2005	TARO PHARMACEUTICAL INDUSTRIES LTD	IMIQUIMOD USP
18782	A	II	9/19/2005	TEVA PHARMACEUTICAL INDUSTRIES LTD	IMIQUIMOD
19009	A	II	12/5/2005	WAVELENGTH ENTERPRISES LTD	IMIQUIMOD
19507	A	II	6/6/2006	TEVA PHARMACEUTICAL INDUSTRIES LTD	IMIQUIMOD
>DMF No.	>Status	>Type	>Submission Date	>Holder	>Subject

Drug Master File Glossary

STATUS OF DMFS

A = Active. This means that the DMF was found acceptable for filing, administratively, and is up-to-date.
I = Inactive
N = Not an assigned number
P = DMF Pending Filing Review

TYPES OF DMFs

Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)
Type II Drug Substance, Drug Substance Intermediate, and Material Used in Their Preparation, or Drug Product
Type III Packaging Material
Type IV Excipient, Colorant, Flavor, Essence, or Material Used in Their Preparation
Type V FDA Accepted Reference Information

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