Drug Master Files for: desipramine hydrochloride

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desipramine hydrochloride Drug Master Files

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DMF No.	Status	Type	Submission Date	Holder	Subject
10461	A	II	9/8/1993	PCAS	DESIPRAMINE HYDROCHLORIDE
3374	A	II	10/4/1978	LUNDBECK PHARMACEUTICALS ITALY SPA	DESIPRAMINE HYDROCHLORIDE
5367	I	II	4/20/1984	FARCHEMIA SRL	DESIPRAMINE HYDROCHLORIDE USP
6012	A	II	9/9/1985	PCAS	DESIPRAMINE HCL
6643	I	II	10/21/1986	IRISH FINE CHEMICALS LTD	DESIPRAMINE HYDROCHLORIDE
6663	I	II	11/5/1986	ACF CHEMIEFARMA NV	DESIPRAMINE 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Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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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