Drug Master Files for: potassium iodide

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potassium iodide Drug Master Files

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DMF No.	Status	Type	Submission Date	Holder	Subject
10234	I	II	5/4/1993	NORTH CHINA PHARMACEUTICAL CORP	PENICILLIN G POTASSIUM CRUDE
10301	I	II	6/11/1993	ARCHER DANIELS MIDLAND CO	POTASSIUM CITRATE MONOHYDRATE
10831	A	II	3/24/1994	YUNG ZIP CHEMICAL IND CO LTD	DICLOFENAC POTASSIUM
11020	I	II	7/31/1994	DERETIL SA	D(-) ALPHA PHENYLGLYCINE DANE SALT ETHYL NPOTASSIUM
11021	I	II	7/31/1994	DERETIL SA	D(-) ALPHA PARAHYDROXY PHENYLGLYCINE DANE SALT METHYL POTASSIUM
11041	I	II	6/24/1994	SMITHKLINE BEECHAM PHARMACEUTICALS CO	PENICILLIN G POTASSIUM, NON-STERILE, TECHNICAL GRADE
11122	I	II	9/30/1994	DSM ANDENO GMBH	R(-)-2-PHENYLGLYCINE DANE SALT (POTASSIUM, ETHYL) (KE)
>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Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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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