Drug Master Files for: Lilly

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Lilly Drug Master Files

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DMF No.	Status	Type	Submission Date	Holder	Subject
1047	I	III	3/31/1967	LILLY RESEARCH LABORATORIES	POLYVINYL CHLORIDE CONTAINERS
11255	I	III	12/19/1994	LILLY FRANCE SAS	QUALITY CONTROL PROCEDURES FOR IN-COMING INSPECTION OF PACKAGING COMPONENTS USED IN FEGERSHEIM FRANCE
13204	I	II	4/30/1998	LILLY RESEARCH LABORATORIES	ERYTHROMYCIN ESTOLATE
13291	I	II	9/1/1998	ELI LILLY AND CO	PENICILLIN G PROCAINE
13331	I	II	9/1/1998	LILLY RESEARCH LABORATORIES	ERYTHROMYCIN ESTOLATE
13332	I	II	9/1/1998	LILLY RESEARCH LABORATORIES	PENICILLIN V POTASSIUM
13333	I	II	9/1/1998	LILLY RESEARCH LABORATORIES	ERYTHROMYCIN ESTOLATE
>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Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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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