Drug Master Files for: NAFCILLIN SODIUM

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NAFCILLIN SODIUM Drug Master Files

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DMF No.	Status	Type	Submission Date	Holder	Subject
13387	I	II	9/1/1998	FERMENTA PRODUCTS INC	NAFCILLIN SODIUM
13554	I	II	9/1/1998	SMITHKLINE BEECHAM PHARMACEUTICALS	NAFCILLIN SODIUM
13653	A	II	9/1/1998	CORDEN PHARMA LATINA SPA	NAFCILLIN SODIUM STERILE
13695	A	II	9/1/1998	ACS DOBFAR SPA	NAFCILLIN SODIUM FOR INJECTION (BULK)
13697	I	II	9/1/1998	ACS DOBFAR SPA	NAFCILLIN SODIUM
19679	I	II	8/10/2006	SANDOZ INDUSTRIAL PRODUCTS SA	NAFCILLIN ACID
>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Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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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