Drug Master Files for: VECURONIUM BROMIDE
✉ Email this page to a colleague
VECURONIUM BROMIDE Drug Master Files
| DMF No. | Status | Type | Submission Date | Holder | Subject |
|---|---|---|---|---|---|
| 12002 | I | II | 6/17/1996 | DIOSYNTH BV | VECURONIUM BROMIDE |
| 12050 | A | II | 7/23/1996 | ZHEJIANG XIANJU PHARMACEUTICAL CO LTD | VECURONIUM BROMIDE |
| 12063 | A | II | 7/26/1996 | EUTICALS SPA | VECURONIUM BROMIDE |
| 20059 | A | II | 12/19/2006 | ASPEN OSS BV | VECURONIUM BROMIDE |
| 4389 | I | II | 12/17/1981 | DIOSYNTH BV | VECURONIUMBROMIDE SECOND SUBMISSION 12-17-81 |
| >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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
