Generated: December 14, 2017
DrugPatentWatch Database Preview
Drug Master Files for: paricalcitol
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|16402||A||II||2/3/2003||CATALENT PHARMA SOLUTIONS LLC||ZEMPLAR (PARICALCITOL) 2 & 4 MCG CAPSULES|
|20865||A||II||9/19/2007||TEVA PHARMACEUTICAL INDUSTRIES LTD||PARICALCITOL USP|
|21255||A||II||1/16/2008||ALP PHARM BEIJING CO LTD||PARICALCITOL USP (NON-STERILE DRUG SUBSTANCE)|
|21880||A||II||8/14/2008||FORMOSA LABORATORIES INC||PARICALCITOL|
|23895||A||II||6/18/2010||NEULAND LABORATORIES LTD||PARICALCITOL, USP|
|24315||A||II||11/30/2010||ABBVIE INC||PARICALCITOL DRUG SUBSTANCE|
|25300||A||II||9/13/2011||DISHMAN NETHERLANDS BV||PARICALCITOL|
|26545||A||II||11/14/2012||SAI LIFE SCIENCES LTD||PARICALCITOL USP, NON-STERILE BULK DRUG|
|27145||A||II||5/4/2013||MICROBIOPHARM JAPAN CO LTD||PARICALCITOL, USP|
|28550||A||II||7/30/2014||CHONGQING HUAPONT PHARMACEUTICAL CO LTD||PARICALCITOL|
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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- Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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
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