Drug Master Files for: fesoterodine fumarate

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fesoterodine fumarate Drug Master Files

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DMF No.	Status	Type	Submission Date	Holder	Subject
25052	A	II	6/16/2011	DIPHARMA FRANCIS SRL	FESOTERODINE FUMARATE
25916	A	II	5/17/2012	CADILA HEALTHCARE LTD	FESOTERODINE FUMARATE
26173	A	II	10/26/2012	SUN PHARMACEUTICAL INDUSTRIES LTD	FESOTERODINE FUMARATE
>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Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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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