Drug Master Files for: esomeprazole magnesium
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esomeprazole magnesium Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 17278 | I | II | 3/31/2004 | DR REDDYS LABORATORIES LTD | ESOMEPRAZOLE MAGNESIUM |
| 18559 | I | II | 8/3/2005 | SUN PHARMACEUTICAL INDUSTRIES LTD | ESOMEPRAZOLE MAGNESIUM (AMORPHOUS, NON-STERILE BULK DRUG SUBSTANCE) |
| 18821 | A | II | 9/28/2005 | CIPLA LTD | ESOMEPRAZOLE MAGNESIUM DIHYDRATE USP |
| 19192 | I | II | 2/21/2006 | DR REDDYS LABORATORIES LTD | ESOMEPRAZOLE MAGNESIUM (AMORPHOUS FORM) |
| 20222 | A | II | 1/31/2007 | GLENMARK PHARMACEUTICALS LTD | ESOMEPRAZOLE |
| 20392 | A | II | 4/2/2007 | GLENMARK PHARMACEUTICALS LTD | ESOMEPRAZOLE POTASSIUM |
| 20457 | A | II | 4/13/2007 | LUPIN LTD | ESOMEPRAZOLE MAGNESIUM DIHYDRATE USP |
| >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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
