Drug Master Files for: sodium iodide i-123
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sodium iodide i-123 Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
10 | I | 2/23/1944 | HERCULES POWDER CO | SODIUM CARBOXYMETHYLCELLULOSE | |
1000 | I | 9/15/1966 | GENERAL FOODS CORP | MONSODIUM DIHYDROGEN PHOSPHATE | |
10003 | A | II | 11/25/1992 | ACS DOBFAR SPA | SODIUM CARBONATE STERILE |
10006 | A | II | 12/15/1992 | FERMION OY | CROMOLYN SODIUM |
10009 | I | V | 7/30/1990 | ASTELLAS PHARMA INC | STERILE PROCESSING FACILITIES FOR CEFTIZOXIME SODIUM, STERILE (BULK) LOCATED IN TAKAOKA, JAPAN |
10030 | I | II | 1/5/1993 | ARES SERONO SA | SODIUM CHLORIDE FOR INJECTION |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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