Drug Master Files for: thiothixene
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thiothixene Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
31839 | A | II | 7/21/2017 | NOVITIUM PHARMA LLC | THIOTHIXENE USP |
5566 | A | II | 9/28/1984 | ORGAPHARM SAS | THIOTHIXENE |
5939 | I | II | 7/26/1985 | ORCHIMIE SA (PRODUITS CHIMIQUES ET BIOCHIMIQUES) | THIOTHIXENE DIHYDROCHLORIDE ANHYDROUS |
6309 | A | II | 5/5/1986 | FINE CHEMICALS CORP PTY LTD | THIOTHIXENE |
6656 | I | II | 9/30/1986 | FINE CHEMICALS CORP PTY LTD | THIOTHIXENE HYDROCHLORIDE |
6776 | I | II | 1/12/1987 | INDUSTRIE CHIMICHE FARMACEUTICHE ITALIANE SPA | THIOTHIXENE BASE AND HC1 |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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