Drug Master Files for: OXACILLIN SODIUM
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OXACILLIN SODIUM Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
13216 | I | II | 4/30/1998 | SANDOZ INDUSTRIAL PRODUCTS SA | OXACILLIN SODIUM |
13221 | I | II | 4/30/1998 | CONSOLIDATED PHARMACEUTICAL GROUP INC | DICLOXACILLIN SODIUM |
13352 | I | II | 9/1/1998 | FERMENTA PRODUCTS INC | DICLOXACILLIN SODIUM |
13386 | I | II | 9/1/1998 | SMITHKLINE BEECHAM PHARMACEUTICALS | OXACILLIN SODIUM MONOHYDRATE |
13429 | I | II | 9/1/1998 | BRISTOL MYERS SQUIBB CO | DICLOXACILLIN SODIUM |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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