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Serving hundreds of leading biopharmaceutical companies globally:

McKesson
Cerilliant
Cipla
Federal Trade Commission
Dow
Farmers Insurance
Johnson and Johnson
Boehringer Ingelheim
Healthtrust

Generated: August 15, 2018

DrugPatentWatch Database Preview

Drug Master Files for: Bristol Myers Squibb

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Bristol Myers Squibb Drug Master Files

DMF No. Status Type Submission Date Holder Subject
1608 I II 11/10/1970 BRISTOL MYERS SQUIBB CO TRIAMCINOLONE AND TRIAMCINOLONE ACETONIDE
2203 I II 12/21/1973 BRISTOL MYERS SQUIBB CO HALCINONIDE BULK
2452 I II 5/21/1975 BRISTOL MYERS SQUIBB CO PHARMACEUTICAL RESEARCH INSTITUTE HYDREA
2467 A II 6/10/1975 BRISTOL MYERS SQUIBB CO WARFARIN SODIUM USP
4056 I II 1/29/1981 BRISTOL MYERS SQUIBB CO JM-9 FOR INJECTION
8141 I V 7/25/1989 BRISTOL MYERS SQUIBB CO FACILITIES FOR PARENTERAL MANUFACTURING (BUILDING 115) LOCATED IN NEW BRUNSWICK, NJ
9081 I II 4/30/1991 BRISTOL MYERS SQUIBB PHARMACEUTICAL RESEARCH INSTITUTE TIPREDANE
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  • Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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:

Chinese Patent Office
Johnson and Johnson
Moodys
UBS
Medtronic
Dow
US Department of Justice
McKesson
Express Scripts

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