Drug Master Files for: isradipine
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isradipine Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
16369 | A | II | 1/21/2003 | SOLARA A PHARMA SCIENCES LTD | ISRADIPINE, USP |
17367 | A | II | 5/5/2004 | CHEMO IBERICA SA | ISRADIPINE |
17384 | A | II | 5/17/2004 | YANGZHOU PHARMACEUTICAL CO LTD | ISRADIPINE (USP26) |
17873 | I | II | 12/7/2004 | SUN PHARMACEUTICAL INDUSTRIES LTD | ISRADIPINE UPS |
19376 | A | II | 4/19/2006 | CHEMOSWED AB | ISRADIPINE |
20749 | I | II | 8/2/2007 | CHEMWERTH INC | ISRADIPINE USP, NON-STERILE BULK DRUG SUBSTANCE |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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