Drug Master Files for: fluphenazine enanthate
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fluphenazine enanthate Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
1434 | I | II | 10/6/1969 | ER SQUIBB AND SONS INC | PROLIXIN ELIXIR (FLUPHENAZINE HYDROCHLORIDE) |
16097 | I | II | 8/12/2002 | FINE CHEMICALS CORP PTY LTD | FLUPHENAZINE DECANOATE OIL(BMS) |
1992 | I | II | 9/7/1972 | SWORDS LABORATORIES LTD | FLUPHENAZINE DECANOATE |
2320 | I | II | 8/27/1974 | SWORDS LABORATORIES LTD | FLUPHENAZINE ENANTHATE N.F. |
2374 | I | II | 12/18/1974 | ER SQUIBB AND SONS INC | FLUPHENAZINE DECANOATE INJ. |
27811 | A | II | 12/23/2013 | TRIFARMA SPA | FLUPHENAZINE DECANOATE |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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