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Serving hundreds of leading biopharmaceutical companies globally:

Fuji
Colorcon
Cipla
Covington
Boehringer Ingelheim
US Department of Justice
Johnson and Johnson
Express Scripts
McKinsey

Generated: July 15, 2018

DrugPatentWatch Database Preview

Drug Master Files for: procyclidine

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procyclidine Drug Master Files

DMF No. Status Type Submission Date Holder Subject
5990 I II 8/19/1985 TRIFARMA SPA PROCYCLIDINE HYDROCHLORIDE USP
DMF No. Status Type Submission Date Holder Subject

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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  • Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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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Serving hundreds of leading biopharmaceutical companies globally:

Teva
Medtronic
Argus Health
Daiichi Sankyo
Cipla
Dow
Federal Trade Commission
Chubb
Mallinckrodt

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