Drug Master Files for: uridine
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uridine Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
11241 | I | II | 12/13/1994 | NAGASE FINE CHEMICALS LTD | 2',3',5' TRI-O-ACETYLURIDINE |
12140 | I | II | 9/20/1996 | PHARMA-WALDHOF GMBH | URIDINE-5'-TRIPHOSPHATE (UTP), THERAPEUTIC GRADE |
12277 | I | II | 12/16/1996 | ROCHE DIAGNOSTICS GMBH | 5-BROMO-2'-DEOXYURIDINE |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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