Drug Master Files for: manganese
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manganese Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
25246 | I | II | 6/20/2011 | TOMITA PHARMACEUTICAL CO LTD | U.S.P. MANGANESE GLUCONATE DIHYDRATE |
30512 | A | II | 4/7/2016 | JOST CHEMICAL CO | MANGANESE SULFATE MONOHYDRATE |
685 | I | V | 9/24/1963 | GRAIN PROCESSING CORP | REQUEST TO MARKET EGGS OF PULLETS FED MANGANESE BACITRACIN (VET) |
686 | I | V | 9/24/1963 | GRAIN PROCESSING CORP | REQUEST TO MARKET STEERS FED MANGANESE BACITRACIN (VET) |
690 | I | V | 10/1/1963 | GRAIN PROCESSING CORP | REQUEST TO MARKET TURKEYS FED MANGANESE BACITRACIN (VET) |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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