Drug Master Files for: VORICONAZOLE
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VORICONAZOLE Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 19996 | A | II | 11/27/2006 | DR REDDYS LABORATORIES LTD | VORICONAZOLE USP |
| 21443 | A | II | 3/18/2008 | MEDICHEM MANUFACTURING MALTA LTD | MED-201950/E (VORICONAZOLE) |
| 21523 | A | II | 4/8/2008 | MSN LABORATORIES PRIVATE LTD | VORICONAZOLE USP [ROUTE CODE - VZ] |
| 23697 | A | II | 4/7/2010 | NEULAND LABORATORIES LTD | VORICONAZOLE USP |
| 24717 | A | II | 3/31/2011 | GLENMARK PHARMACEUTICALS LTD | VORICONAZOLE 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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
