Drug Master Files for: MECLOFENAMATE SODIUM
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MECLOFENAMATE SODIUM Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 22795 | A | II | 3/23/2009 | YUNG SHIN PHARMACEUTICAL INDUSTRIAL CO LTD | MECLOFENAMATE SODIUM |
| 3709 | I | II | 2/1/1980 | UPJOHN CO | SODIUM MECLOFENAMATE |
| 5584 | A | II | 11/13/1984 | ALBEMARLE CORP | MECLOFENAMATE SODIUM USP |
| 5741 | I | II | 3/11/1985 | PROFARMACO SRL | MECLOFENAMATE SODIUM |
| 6224 | I | II | 2/27/1986 | FINE CHEMICALS CORP | MECLOFENAMATE SODIUM |
| 6857 | I | II | 3/9/1987 | CAMBREX PROFARMACO MILANO SRL | MECLOFENAMATE SODIUM |
| 6871 | I | II | 3/13/1987 | QUIMICA SINTETICA SA | MECLOFENAMATE SODIUM USP |
| >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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
