Drug Master Files for: VENLAFAXINE HYDROCHLORIDE
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VENLAFAXINE HYDROCHLORIDE Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 10005 | I | II | 12/15/1992 | ALZA CORP | GITS (VENLAFAXINE HYDROCHLORIDE) |
| 12346 | A | II | 1/29/1997 | ZACH SYSTEM SA | VENLAFAXINE HYDROCHLORIDE |
| 15923 | A | II | 4/2/2002 | SIEGFRIED LTD | O-DESMETHYLVENLAFAXINE SUCCINATE MONOHYDRATE |
| 16084 | I | II | 8/5/2002 | MEDICHEM SA | VENLAFAXINE HCL |
| 16188 | A | II | 10/4/2002 | UQUIFA MEXICO SA DE CV | VENLAFAXINE HYDROCHLORIDE |
| 16281 | A | II | 12/2/2002 | TEVA PHARMACEUTICAL INDUSTRIES LTD | VENLAFAXINE HYDROCHLORIDE |
| 16551 | I | II | 4/29/2003 | ALEMBIC PHARMACEUTICALS LTD | VENLAFAXINE 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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
