Drug Master Files for: IMIQUIMOD
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IMIQUIMOD Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 18031 | A | II | 1/26/2005 | TARO PHARMACEUTICAL INDUSTRIES LTD | IMIQUIMOD USP |
| 18782 | A | II | 9/19/2005 | TEVA PHARMACEUTICAL INDUSTRIES LTD | IMIQUIMOD |
| 19009 | A | II | 12/5/2005 | WAVELENGTH ENTERPRISES LTD | IMIQUIMOD |
| 19507 | A | II | 6/6/2006 | TEVA PHARMACEUTICAL INDUSTRIES LTD | IMIQUIMOD |
| 19735 | A | II | 9/6/2006 | GLENMARK PHARMACEUTICALS LTD | IMIQUIMOD USP |
| 20247 | A | II | 2/7/2007 | INTERQUIM SA | IMIQUIMOD |
| >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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
