Drug Master Files for: tranylcypromine sulfate
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tranylcypromine sulfate Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 10317 | I | II | 6/25/1993 | LONZA RIVERSIDE | TRANYLCYPROMINE SULFATE |
| 16522 | A | II | 2/27/2003 | TRIFARMA SPA | TRANYLCYPROMINE SULFATE |
| 26808 | A | II | 2/18/2013 | CENTAUR PHARMACEUTICALS PRIVATE LTD | TRANYLCYPROMINE SULFATE USP |
| 4680 | I | II | 10/28/1982 | SMITH KLINE & FRENCH LABS DIV SMITHKLINE BECKMAN CORP | TRANYLCYPROMINE SULFATE |
| 7132 | I | II | 9/4/1987 | ALCHYMARS SPA | TRANYLCYPROMINE SULFATE USP |
| 716 | I | II | 11/4/1963 | SMITH KLINE & FRENCH LABS DIV SMITHKLINE BECKMAN CORP | SKF 385 TRANYLCYPROMINE (VET) |
| >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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
