Drug Master Files for: NANDROLONE PHENPROPIONATE

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NANDROLONE PHENPROPIONATE Drug Master Files

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DMF No.	Status	Type	Submission Date	Holder	Subject
21762	A	II	7/3/2008	ASPEN OSS BV	NANDROLONE DECANOATE
2251	I	II	3/18/1974	ORGANON INC	NORANDROS TENEDIONE (NANDROLONE)
2399	I	II	2/11/1975	ROUSSELL UCLAF	19-NOR-ANDROSTENEDIONE (NANDROLONE)
24883	I	II	11/21/2011	RELIANCE LIFE SCIENCES PVT LTD	NANDROLONE DECANOATE USP
3225	I	II	5/25/1978	ORMA ISTITUDO TERAPEUTICO	NANDROLONE PHENYLPROPIONATE
3229	I	II	5/28/1978	ORMA ISTITUDO TERAPEUTICO	NANDROLONE DECANOATE
>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Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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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