Drug Master Files for: chymotrypsin
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chymotrypsin Drug Master Files
DMF No. | Status | Type | Submission Date | Holder | Subject |
---|---|---|---|---|---|
26454 | A | II | 8/30/2012 | BEIJING GEYUAN TIANRUN BIO TECH CO LTD | CHYMOTRYPSIN (NON-STERILE, BULK FORM) |
2837 | I | II | 1/27/1977 | WAITAKI INTERNATIONAL BIOSCIENCES SUB WAITAKI CANADA LTD | CHYMOTRYPSIN AND/OR TRYPSIN |
28779 | A | II | 8/15/2014 | ENZYMEKING BIOTECHNOLOGY CO LTD | CHYMOTRYPSIN |
31033 | A | II | 9/19/2016 | ZHEJIANG FENG'AN BIO-PHARMACEUTICAL CO LTD | CHYMOTRYPSIN |
351 | I | II | 11/2/1959 | PRINCETON LAB PRODS CO | TRYPSIN, CHYMOTRYPSIN & RIBONUCLEASE - 'G PROCEDURES & ASSAYS |
367 | I | II | 2/17/1960 | WAITAKI INTERNATIONAL BIOSCIENCES SUB WAITAKI CANADA LTD | TRYPSIN & a - CHYMOTRYPSIN - PREPARTION & ASSAY METHODS |
407 | I | II | 11/7/1960 | WORTHINGTON BIOCHEM CORP | CHYMOTRYPSIN (MANUF PROCEDURE) |
>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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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