Drug Master Files for: PFIZER

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PFIZER Drug Master Files

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DMF No.	Status	Type	Submission Date	Holder	Subject
1022	I		1/19/1967	CHAS PFIZER AND CO INC	METAMINE
104	I		1/1/1940	CHAS PFIZER AND CO INC	STREPTOMYCIN HYDRAZIDE ISONICOTINYL
10447	I	II	8/26/1993	PHARMACIA AND UPJOHN SUB PFIZER INC	HYDROCORTISONE BUTYRATE
10536	I	II	10/18/1993	PHARMACIA AND UPJOHN SUB PFIZER INC	ESTRADIOL
10664	I	II	1/5/1994	PFIZER IRELAND PHARMACEUTICALS	FEDOTOZINE TARTRATE
11848	A	II	2/8/1996	PHARMACIA AND UPJOHN CO WHOLLY OWNED SUB PFIZER INC	BETAMETHYL EPOXIDE
>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Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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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