Drug Master Files for: pancuronium bromide
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pancuronium bromide Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
10247 | I | II | 5/17/1993 | DIOSYNTH BV | PANCURONIUM BROMIDE |
16052 | A | II | 7/15/2002 | EUTICALS SPA | PANCURONIUM BROMIDE |
6817 | A | II | 1/23/1987 | TEVA PHARMACEUTICAL INDUSTRIES LTD | PANCURONIUM BROMIDE |
7121 | I | II | 8/26/1987 | SCHERING AG | PANCURONIUM BROMIDE |
8665 | I | II | 7/23/1990 | DIOSYNTH BV | PANCURONIUM BROMIDE |
9037 | I | II | 3/29/1991 | OMNICHEM NV | PANCURONIUM BROMIDE |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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