Drug Master Files for: trifluoperazine
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trifluoperazine Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
2594 | I | II | 1/23/1976 | PHENCHEM INDUSTRIES LTD | TRIFLUOPERAZINE HCL |
2853 | A | II | 2/1/1977 | TRIFARMA SPA | TRIFLUOPERAZINE HYDROCHLORIDE |
3080 | I | II | 11/29/1977 | RHONE POULENC RORER PHARMACEUTICALS INC | TRIFLUOPERAZINE CHLORHYDRATE |
3515 | I | II | 4/2/1979 | IRISH FINE CHEMICALS LTD | TRIFLUOPERAZINE |
4342 | I | II | 10/19/1981 | ACIC LTD | PROCEDURES FOR THE MANUF OF TRIFLUOPERAZINE HCL |
4788 | I | II | 1/20/1983 | SMITH KLINE AND FRENCH LABORATORIES | TRIFLUOPERAZINE HYDROCHLORIDE |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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