Drug Master Files for: nimodipine

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nimodipine Drug Master Files

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DMF No.	Status	Type	Submission Date	Holder	Subject
14979	A	II	7/26/2000	LUSOCHIMICA SPA	NIMODIPINE
15598	I	II	8/27/2001	CATALENT PHARMA SOLUTIONS LLC	NIMODIPINE 30MG SOFTGEL CAPSULES
16951	A	II	11/3/2003	UNION QUIMICO FARMACEUTICA SA (UQUIFA SA)	NIMODIPINE (MICRONIZED)
17849	I	II	11/22/2004	USV LTD	NIMODIPINE USP
>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Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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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