Drug Master Files for: fesoterodine fumarate
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fesoterodine fumarate Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 25052 | A | II | 6/16/2011 | DIPHARMA FRANCIS SRL | FESOTERODINE FUMARATE |
| 25916 | A | II | 5/17/2012 | CADILA HEALTHCARE LTD | FESOTERODINE FUMARATE |
| 26173 | A | II | 10/26/2012 | SUN PHARMACEUTICAL INDUSTRIES LTD | FESOTERODINE FUMARATE |
| 26241 | A | II | 9/4/2012 | ALEMBIC PHARMACEUTICALS LTD | FESOTERODINE FUMARATE |
| 26275 | A | II | 10/31/2012 | LUPIN LTD | FESOTERODINE FUMARATE |
| >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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
