Drug Master Files for: DIPIVEFRIN HYDROCHLORIDE
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DIPIVEFRIN HYDROCHLORIDE Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
12242 | I | II | 12/2/1996 | PCAS | DIPIVEFRIN HYDROCHLORIDE |
5726 | I | II | 2/4/1985 | KLINGE PHARMA CO | DIPIVEFRINE HCL. |
8175 | I | II | 7/19/1989 | PHARMECO LABORATORIES INC | DIPIVEFRIN HCL |
9277 | I | II | 8/6/1991 | PHARMECO LABORATORIES INC | DIPIVEFRIN |
9552 | I | II | 2/20/1992 | SUMITOMO CHEMICAL CO LTD | DIPIVEFRIN 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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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