Drug Master Files for: MOEXIPRIL HYDROCHLORIDE

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MOEXIPRIL HYDROCHLORIDE Drug Master Files

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DMF No.	Status	Type	Submission Date	Holder	Subject
10520	I	II	9/30/1993	ORGAMOL SA	MOEXIPRIL HYDROCHLORIDE
15172	A	II	12/6/2000	ESTEVE QUIMICA SA	MOEXIPRIL HYDROCHLORIDE
16670	I	II	6/25/2003	UCB MANUFACTURING IRELAND LTD	MOEXIPRIL HYDROCHLORIDE
>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Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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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