Drug Master Files for: CEFUROXIME SODIUM

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CEFUROXIME SODIUM Drug Master Files

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DMF No.	Status	Type	Submission Date	Holder	Subject
10154	A	II	3/1/1991	ACS DOBFAR SPA	CEFUROXIME ACID
13205	A	II	4/30/1998	ACS DOBFAR SPA	CEFUROXIME SODIUM (STERILE BULK)
13675	I	II	9/1/1998	ELI LILLY AND CO	CEFUROXIME SODIUM
14010	I	II	3/4/1999	FARMABIOS SRL	CEFUROXIME
14058	I	II	4/7/1999	SUN PHARMACEUTICAL INDUSTRIES LTD	CEFUROXIME AXETIL USP (CRYSTALLINE)
14074	I	II	4/7/1999	RANBAXY LABORATORIES LTD	CEFUROXIME AXETIL
>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Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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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