Drug Master Files for: fenoprofen calcium
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fenoprofen calcium Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 20498 | A | II | 4/26/2007 | SUVEN LIFE SCIENCES LTD | FENOPROFEN CALCIUM USP |
| 22105 | I | II | 10/22/2008 | EMCURE PHARMACEUTICALS LTD | FENOPROFEN CALCIUM USP |
| 5102 | I | II | 9/16/1983 | ELI LILLY AND CO | FENOPROFEN CALCIUM, BULK FORM |
| 6843 | A | II | 3/3/1987 | ALBEMARLE CORP | FENOPROFEN CALCIUM, USP+BP |
| 6904 | I | II | 4/3/1987 | BLASCHIM SPA | FENOPROFEN CALCIUM |
| 6932 | I | II | 4/14/1987 | CAMBREX PROFARMACO MILANO SRL | FENOPROFEN CALCIUM |
| 7041 | I | II | 6/30/1987 | FARMOS GROUP LTD MEDIPOLAR | FENOPROFEN CALCIUM |
| >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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
