Drug Master Files for: liothyronine sodium

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liothyronine sodium Drug Master Files

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DMF No.	Status	Type	Submission Date	Holder	Subject
19467	A	II	5/19/2006	PEPTIDO GMBH	LIOTHYRONINE SODIUM
22437	A	II	3/16/2009	SUN PHARMACEUTICAL INDUSTRIES LTD	SUN 8016 (LIOTHYRONINE SODIUM USP)
30942	A	II	9/30/2016	AZICO BIOPHORE INDIA PVT LTD	LIOTHYRONINE 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Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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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