Drug Master Files for: CLOXACILLIN SODIUM
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CLOXACILLIN SODIUM Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 13221 | I | II | 4/30/1998 | CONSOLIDATED PHARMACEUTICAL GROUP INC | DICLOXACILLIN SODIUM |
| 13352 | I | II | 9/1/1998 | FERMENTA PRODUCTS INC | DICLOXACILLIN SODIUM |
| 13429 | I | II | 9/1/1998 | BRISTOL MYERS SQUIBB CO | DICLOXACILLIN SODIUM |
| 13431 | I | II | 9/1/1998 | BRISTOL MYERS SQUIBB CO | DICLOXACILLIN SODIUM |
| 13434 | I | II | 9/1/1998 | BRISTOL MYERS SQUIBB CO | CLOXACILLIN SODIUM |
| 13474 | I | II | 9/1/1998 | SMITHKLINE BEECHAM PHARMACEUTICALS | CLOXACILLIN SODIUM |
| 13476 | I | II | 9/1/1998 | SMITHKLINE BEECHAM PHARMACEUTICALS | CLOXACILLIN BENZATHINE |
| >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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
