Drug Master Files for: ritodrine hydrochloride

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ritodrine hydrochloride Drug Master Files

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DMF No.	Status	Type	Submission Date	Holder	Subject
10315	I	II	6/16/1993	LUSOCHIMICA SPA	RITODRINE HYDROCHLORIDE
3490	I	II	3/6/1979	DUPHAR BV	RITODRINE HCL
4527	I	II	4/26/1982	DUPHAR BV	YUTOPAR (RITODRINE HCL) TABLETS & INJECTION FORMS,OLST,HOLLAND
6173	I	II	1/3/1986	ORION CORP LTD	RITODRINE HCL
6264	I	II	4/14/1986	OY STAR AB	RITODRINE HCL
>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Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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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