Drug Master Files for: apomorphine hydrochloride
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apomorphine hydrochloride Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
12818 | A | II | 1/7/1998 | SANOFI CHIMIE | APOMORPHINE HYDROCHLORIDE |
13188 | A | II | 9/11/1998 | MACFARLAN SMITH LTD | APOMORPHINE HYDROCHLORIDE |
6966 | I | II | 5/8/1987 | SIGMA F AND D DIV LTD | APOMORPHINE HCl |
8999 | I | II | 3/4/1991 | DIOSYNTH BV | APOMORPHINE HYDROCHLORIDE |
9336 | I | II | 9/6/1991 | LABORATOIRE AGUETTANT PARC SCIENTIFIC TONY GARNIER RUE ALEXANDER FLEMMING | APOMORPHINE |
9338 | I | II | 9/6/1991 | LABORATOIRE AGUETTANT PARC SCIENTIFIC TONY GARNIER RUE ALEXANDER FLEMMING | FACILITIES AND PROCEDURES FOR THE G. OF APOMORPHINE, FRANCE |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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