Drug Master Files for: Ciba
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Ciba Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
1019 | I | 1/5/1967 | CIBA PHARMACEUTICAL CO DIV CIBA GEIGY CORP | ORISUL TABS, SUSPENSION & SUSPENSION FOR CHILDREN | |
10394 | I | I | 8/2/1993 | CIBA GEIGY MEXICANA SA DE CV | FACILITY AND OPERATING PROCEDURES IN PUEBLA, MEXICO |
11850 | I | I | 2/5/1996 | CIBA GEIGY CORP PHARMACEUTICALS DIV | MANUFACTURING SITE, FACILITIES, PERSONNEL, AND GENERAL OPERATING PROCEDURES BY CIBA-GEIGY SPA IN TORRE ANNUNIATA (NAPLES) ITALY. |
1201 | I | 7/15/1956 | CIBA PHARMACEUTICAL CO DIV CIBA GEIGY CORP | SYNACTHEN (BA-30920) | |
12410 | I | V | 2/28/1997 | CIBA VISION STERILE MANUFACTURING | STERILE |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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