Drug Master Files for: nedocromil sodium

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nedocromil sodium Drug Master Files

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DMF No.	Status	Type	Submission Date	Holder	Subject
10944	A	II	6/17/1994	AVENTIS PHARMA MANUFACTURING PTE LTD	NEDOCROMIL SODIUM
21169	I	II	12/19/2007	CHEMO IBERICA SA MADRID	Nedocromil Disodium
6513	I	II	7/30/1986	FISONS PHARMACEUTICAL LTD	NEDOCROMIL SODIUM
>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Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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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