Drug Master Files for: NORTRIPTYLINE HYDROCHLORIDE

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NORTRIPTYLINE HYDROCHLORIDE Drug Master Files

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DMF No.	Status	Type	Submission Date	Holder	Subject
21330	A	II	1/31/2008	TEVA PHARMACEUTICAL INDUSTRIES LTD	NORTRIPTYLINE HYDROCHLORIDE USP
25380	A	II	10/7/2011	CENTAUR PHARMACEUTICALS PVT LTD	NORTRIPTYLINE HCI USP
2890	I	II	3/18/1977	LILLY RESEARCH LABORATORIES DIV ELI LILLY AND CO	NORTRIPTYLINE HCL CAPSULES
2891	I	II	3/18/1977	LILLY RESEARCH LABORATORIES DIV ELI LILLY AND CO	NORTRIPTYLINE HCL SOLUTION
>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Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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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