Drug Master Files for: Siegfried
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Siegfried Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
10340 | A | II | 6/28/1993 | SIEGFRIED PHARMACHEMIKALIEN MINDEN GMBH | SELEGILINE HYDROCHLORIDE |
1049 | A | II | 3/21/1967 | SIEGFRIED USA LLC | PHENOBARBITAL SODIUM USP |
1050 | A | II | 3/22/1967 | SIEGFRIED USA LLC | SECOBARBITAL SODIUM USP |
1051 | A | II | 3/23/1967 | SIEGFRIED USA LLC | AMOBARBITAL SODIUM USP |
11023 | A | II | 8/2/1994 | SIEGFRIED PHARMACHEMIKALIEN MINDEN GMBH | DOBUTAMINE HYDROCHLORIDE |
11104 | I | II | 9/28/1994 | SIEGFRIED LTD | SELEGILINE HYDROCHLORIDE |
1166 | A | II | 4/9/1968 | SIEGFRIED USA LLC | BUTALBITAL 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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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