Drug Master Files for: CARBIDOPA
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CARBIDOPA Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 11246 | I | II | 12/8/1994 | KNOLL AG | CARBIDOPA |
| 17846 | A | II | 11/20/2004 | DIVIS LABORATORIES LTD | CARBIDOPA USP |
| 18245 | I | II | 4/5/2005 | SMRUTHI ORGANICS LTD | CARBIDOPA USP |
| 19899 | A | II | 10/16/2006 | ZHEJIANG CHIRAL MEDICINE CHEMICALS CO LTD | CARBIDOPA |
| 22424 | A | II | 12/10/2008 | ZHEJIANG WILD WIND PHARMACEUTICAL CO LTD | CARBIDOPA (NON-STERILE, BULK FORM) |
| 25563 | A | II | 12/7/2011 | GLOCHEM INDUSTRIES PRIVATE LTD | CARBIDOPA |
| >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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
