Drug Master Files for: selegiline hydrochloride

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selegiline hydrochloride Drug Master Files

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DMF No.	Status	Type	Submission Date	Holder	Subject
10036	I	II	12/30/1992	ARENOL CHEMICAL CORP	SELEGILINE (DEPRENYL) HYDROCHLORIDE
10235	I	II	5/5/1993	TEVA PHARMACEUTICAL INDUSTRIES LTD	SELEGILINE HYDROCHLORIDE
10340	A	II	6/28/1993	SIEGFRIED PHARMACHEMIKALIEN MINDEN GMBH	SELEGILINE HYDROCHLORIDE
10529	I	II	10/14/1993	IROTEC LABORATORIES	SELEGILINE HYDROCHLORIDE
10821	I	II	4/12/1994	CHINOIN PHARMACEUTCIAL AND CHEMICAL WORKS CO LTD	FACILITY FOR THE MANUFACTURE OF SELEGILINE HYDROCHLORIDE IN BUDAPEST, HUNGARY
>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Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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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