Drug Master Files for: ETHAMBUTOL HYDROCHLORIDE
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ETHAMBUTOL HYDROCHLORIDE Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 11171 | A | II | 10/31/1994 | CADILA PHARMACEUTICALS LTD | ETHAMBUTOL HYDROCHLORIDE USP |
| 16466 | I | II | 3/13/2003 | CADILA PHARMACEUTICALS LTD | ETHAMBUTOL HYDROCHLORIDE USP SPECIAL |
| 20404 | A | II | 3/30/2007 | LUPIN LTD | ETHAMBUTOL HYDROCHLORIDE USP |
| 6382 | I | II | 5/27/1986 | CHINOIN PHARMACEUTCIAL AND CHEMICAL WORKS CO LTD | ETHAMBUTOL HYDROCHLORIDE |
| 8582 | I | II | 5/28/1990 | DELMAR CHEMICALS INC | ETHAMBUTOL DIHYDROCHLORIDE |
| >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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
