Drug Master Files for: DESOXIMETASONE
DESOXIMETASONE Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 11018 | I | II | 8/4/1994 | TARO PHARMACEUTICAL INDUSTRIES LTD | DESOXIMETASONE |
| 13861 | A | II | 11/25/1998 | TARO PHARMACEUTICAL INDUSTRIES LTD | DESOXIMETASONE USP |
| 14852 | A | II | 4/28/2000 | SANOFI CHIMIE | DESOXIMETASONE USP, MICRONIZED |
| 17759 | A | II | 10/18/2004 | FARMABIOS SPA | DESOXIMETASONE |
| 22400 | A | II | 1/12/2009 | SYMBIOTEC PHARMALAB PRIVATE LTD | DESOXIMETASONE USP (MICRONIZED) |
| 26841 | A | II | 3/29/2013 | TARO PHARMACEUTICAL INDUSTRIES LTD | DESOXIMETASONE USP, MICRONIZED |
| 7424 | I | II | 4/5/1988 | SOCIETA ITALIANA CORTICOSTEROIDI SPA | DESOXIMETASONE |
| >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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
