Drug Master Files for: THALLOUS CHLORIDE TL-201
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THALLOUS CHLORIDE TL-201 Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 15761 | I | II | 11/30/2001 | MDS NORDION SA | THALLOUS (T1-201) CHLORIDE |
| 2601 | I | II | 2/10/1976 | MALLINCKRODT INC | THALLOUS CHLORIDE (T1-201) |
| 3746 | A | II | 3/10/1980 | GE HEALTHCARE INC | THALLOUS CL (TL-201) (CYCLOTRON OPERATION) |
| 4128 | A | II | 3/31/1981 | CURIUM US LLC | THALLOUS CHLORIDE TI 201 |
| 4316 | I | V | 11/6/1981 | TOXICOL SISA INC | PRROGENICITY TESTING OF THALLOUS CHLORIDE T1-201 INJECT |
| 8035 | I | II | 4/27/1989 | IMAGENTS INC | RADIOCHEMICAL THALLOUS CHLORIDE TL-201 |
| >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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
