Drug Master Files for: prednisolone sodium phosphate

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prednisolone sodium phosphate Drug Master Files

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DMF No.	Status	Type	Submission Date	Holder	Subject
11218	I	II	10/7/1994	TIANJIN PHARMACEUTICAL CORP	PREDNISOLONE
1432	I	II	9/18/1969	PHARMACIA AND UPJOHN SUB PFIZER INC	PREDNISOLONE USP
1454	I	II	12/12/1969	UPJOHN CO	FLUPREDNISOLONE & FLUPREDNISOLONE ACETATE
15652	I	II	10/8/2001	SANOFI CHIMIE	PREDNISOLONE SODIUM METASULFOBENZOATE
15912	I	II	3/25/2002	PHARMACIA AND UPJOHN SUB PFIZER INC	METHYLPREDNISOLONE 100MG TABLETS
>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Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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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