Drug Master Files for: oxandrolone
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oxandrolone Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
15427 | I | II | 5/17/2001 | GEDEON RICHTER PLC | OXANDROLONE |
16217 | I | II | 10/21/2002 | OLON SPA | OXANDROLONE |
16598 | A | II | 5/22/2003 | CEDARBURG PHARMACEUTICALS INC | OXANDROLONE USP |
16849 | A | II | 9/16/2003 | EUTICALS SPA | OXANDROLONE USP |
16938 | I | II | 10/31/2003 | SCINOPHARM TAIWAN LTD | OXANDROLONE |
17459 | I | II | 6/9/2004 | NV ORGANON | OXANDROLONE |
17962 | A | II | 1/5/2005 | TRIFARMA SPA | OXANDROLONE 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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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