Drug Master Files for: pimecrolimus
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pimecrolimus Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
29390 | A | II | 9/30/2015 | BIOCON LTD | PIMECROLIMUS |
29433 | A | II | 5/28/2015 | BRIGHTGENE BIOMEDICAL TECHNOLOGY CO LTD | PIMECROLIMUS INTERMEDIATE ASCOMYCIN |
29658 | A | II | 9/15/2015 | CONCORD BIOTECH LTD | PIMECROLIMUS |
30090 | A | II | 12/30/2015 | BRIGHTGENE BIOMEDICAL TECHNOLOGY CO LTD | PIMECROLIMUS (NON-STERILE, API) |
32348 | A | II | 12/14/2017 | EUTICALS SPA | PIMECROLIMUS |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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