Drug Master Files for: flavoxate hydrochloride
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flavoxate hydrochloride Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 13179 | I | II | 9/8/1998 | YAMAMOTO CHEMICAL INDUSTRIES CO LTD | FLAVOXATE HYDROCHLORIDE JP XIII |
| 15613 | I | II | 9/5/2001 | SCINOPHARM TAIWAN LTD | FLAVOXATE HYDROCHLORIDE |
| 16336 | I | II | 12/17/2002 | DAITO CORP | FLAVOXATE HYDROCHLORIDE JP14 |
| 4430 | I | II | 2/3/1982 | LONZA INC | FLAVOXATE HYDROCHLORIDE |
| 6494 | A | II | 7/31/1986 | RECORDATI INDUSTRIA CHIMICA E FARMACEUTICA SPA | FLAVOXATE HYDROCHLORIDE |
| 6879 | I | II | 3/10/1987 | SANKYO CHEMICAL INDUSTRIES INC | FLAVOXATE HYDROCHLORIDE |
| 8443 | I | II | 2/28/1990 | SUMIKA FINE CHEMICALS CO LTD | FLAVOXATE HYDROCHLORIDE |
| >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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
