Drug Master Files for: HALOBETASOL PROPIONATE
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HALOBETASOL PROPIONATE Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 16329 | I | II | 12/16/2002 | SAFC INC | HALOBETASOL PROPIONATE (HBS) |
| 16856 | A | II | 9/22/2003 | WAVELENGTH ENTERPRISES LTD | HALOBETASOL PROPIONATE |
| 16861 | A | II | 9/23/2003 | STERLING SPA | HALOBETASOL PROPIONATE |
| 16944 | I | II | 11/6/2003 | TEVA PHARMACEUTICAL INDUSTRIES LTD | HALOBETASOL PROPIONATE |
| 16953 | A | II | 11/13/2003 | HOVIONE FARMACIENCIA SA | HALOBETASOL PROPIONATE |
| 17529 | A | II | 7/14/2004 | TARO PHARMACEUTICAL INDUSTRIES LTD | HALOBETASOL PROPIONATE USP, MICRONIZED |
| 18566 | A | II | 8/4/2005 | TRIFARMA SPA | HALOBETASOL PROPIONATE |
| >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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
