Drug Master Files for: TOBRAMYCIN SULFATE
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TOBRAMYCIN SULFATE Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
12128 | I | II | 9/12/1996 | GUANGDONG QINGYUAN NEW NORTH RIVER PHARMACEUTICAL CO LTD | TOBRAMYCIN |
12151 | I | II | 10/1/1996 | GUANGDONG QINGYUAN NEW NORTH RIVER PHARMACEUTICAL CO LTD | MANUFACTURING FACILITIES FOR TOBRAMYCIN PHARMACEUTICAL CO., LTD. |
13513 | I | II | 9/1/1998 | LILLY RESEARCH LABORATORIES | TOBRAMYCIN SULFATE |
13713 | A | II | 9/1/1998 | TEVA PHARMACEUTICAL INDUSTRIES LTD | TOBRAMYCIN |
13739 | I | II | 9/1/1998 | PHARMACHIM ECONOMIC CORP | TOBRAMYCIN |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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