Drug Master Files for: DEFEROXAMINE MESYLATE
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DEFEROXAMINE MESYLATE Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
10041 | I | II | 1/13/1993 | PHARMACIA AND UPJOHN | DEFEROXAMINE MESYLATE |
12241 | A | II | 12/2/1996 | TEVA PHARMACEUTICAL INDUSTRIES LTD | DEFEROXAMINE MESYLATE |
16653 | I | II | 6/16/2003 | MYTHEN SPA | DEFEROXAMINE MESYLATE |
18459 | A | II | 6/27/2005 | EXCELLA GMBH AND CO KG | DEFEROXAMINE MESYLATE |
19052 | I | II | 12/17/2005 | MYTHEN SPA | DEFEROXAMINE MESYLATE NT |
20253 | I | II | 2/9/2007 | NAVINTA LLC | DEFEROXAMINE MESYLATE USP |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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