Drug Master Files for: halcinonide
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halcinonide Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 18352 | A | II | 5/13/2005 | FARMABIOS SPA | HALCINONIDE |
| 2203 | I | II | 12/21/1973 | BRISTOL MYERS SQUIBB CO | HALCINONIDE BULK |
| 2579 | I | II | 12/26/1975 | MANUFACTURING ENTERPRISES INC | HALOG (HALCINONIDE) 0.1% SOL. |
| 2580 | I | II | 12/26/1975 | WESTWOOD SQUIBB PHARMACEUTICALS INC | HALOG (HALCINONIDE 0.1% OINTMENT) |
| 3393 | I | II | 11/22/1978 | MANUFACTURING ENTERPRISES INC | HALOG-H CREAM (HALCINONIDE CREAM 0.1%) |
| 7448 | I | II | 4/15/1988 | SOCIETA ITALIANA CORTICOSTEROIDI SPA | HALCINONIDE |
| 8335 | I | II | 12/9/1989 | FARMABOIS | HALCINONIDE |
| >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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
