Drug Master Files for: MUPIROCIN
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MUPIROCIN Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 13961 | I | II | 1/29/1999 | GLAXOSMITHKLINE LLC | MUPIROCIN FREE ACID AND MUPIROCIN CALCIUM (NON-STERILE) |
| 14040 | A | II | 3/11/1999 | TEVA PHARMACEUTICAL INDUSTRIES LTD | MUPIROCIN |
| 15287 | A | II | 2/12/2001 | TEVA PHARMACEUTICAL INDUSTRIES LTD | MUPIROCIN |
| 16541 | I | II | 4/15/2003 | CHEMAGIS LTD | MUPIROCIN CALCIUM (AMORPHOUS) |
| 20041 | A | II | 12/14/2006 | TEVA PHARMACEUTICAL INDUSTRIES LTD | MUPIROCIN CALCIUM |
| >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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
