Drug Master Files for: Cadila
✉ Email this page to a colleague
Cadila Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
11171 | A | II | 10/31/1994 | CADILA PHARMACEUTICALS LTD | ETHAMBUTOL HYDROCHLORIDE USP |
12977 | A | II | 5/2/1998 | CADILA HEALTHCARE LTD | WARFARIN SODIUM USP (CRYSTALLINE CLATHRATE) |
14210 | A | II | 6/14/1999 | CADILA HEALTHCARE LTD | ATENOLOL USP |
14253 | A | II | 6/29/1999 | CADILA PHARMACEUTICALS LTD | FLUOXETINE HYDROCHLORIDE USP |
14264 | I | II | 6/29/1999 | CADILA PHARMACEUTICALS LTD | G SITE FACILITIES PROCEDURES AND PERSONEL FOR ANKLESHWAR SITE IN GUJARAT INDIA |
14910 | I | II | 6/1/2000 | CADILA HEALTHCARE LTD | DEFERIPRONE |
14977 | A | II | 8/1/2000 | CADILA HEALTHCARE LTD | HYDROXYCHLOROQUINE SULFATE 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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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