Drug Master Files for: RAMIPRIL

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RAMIPRIL Drug Master Files

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DMF No.	Status	Type	Submission Date	Holder	Subject
15208	A	II	12/19/2000	SANOFI AVENTIS DEUTSCHLAND GMBH	RAMIPRIL
16193	A	II	10/17/2002	DR REDDYS LABORATORIES LTD	RAMIPRIL USP
16647	A	II	6/10/2003	NEULAND LABORATORIES LTD	RAMIPRIL USP
16900	I	II	10/13/2003	ESTEVE QUIMICA SA	RAMIPRIL
>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Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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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