Drug Master Files for: Interpharm
✉ Email this page to a colleague
Interpharm Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
10576 | I | II | 11/18/1993 | INTERPHARMA PRAHA AS | IODIPAMIDE DRUG SUBSTANCE |
16998 | A | II | 12/1/2003 | INTERPHARMA PRAHA AS | DIINDOLYLMETHANE (DIM) |
21171 | I | II | 10/10/2007 | INTERPHARMA PRAHA AS | Trospium Chloride |
26641 | A | II | 1/24/2013 | INTERPHARMA PRAHA AS | IOHEXOL DRUG SUBSTANCE, FOR ORAL PRODUCTS |
5577 | I | I | 11/5/1984 | INTERPHARM PHARMACEUTICAL PRODUCTS INC | BIO-CHEMICL LABS.,INC.,DIV.OF INTERPHARM PHARM PROD |
6056 | I | II | 10/2/1985 | INTERPHARM INC | FOR PLAINVIEW,N.Y. |
8705 | I | II | 8/17/1990 | INTERPHARM LABORATORIES LTD | FACILITY FOR G. HUMAN INTERFERON, BETA IN NESS-ZIONA, ISRAEL |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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