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Fuji
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Generated: January 19, 2019

DrugPatentWatch Database Preview

Drug Master Files for: Lilly

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Lilly Drug Master Files

DMF No. Status Type Submission Date Holder Subject
1047 I III 3/31/1967 LILLY RESEARCH LABORATORIES POLYVINYL CHLORIDE CONTAINERS
11255 I III 12/19/1994 LILLY FRANCE SAS QUALITY CONTROL PROCEDURES FOR IN-COMING INSPECTION OF PACKAGING COMPONENTS USED IN FEGERSHEIM FRANCE
13204 I II 4/30/1998 LILLY RESEARCH LABORATORIES ERYTHROMYCIN ESTOLATE
13291 I II 9/1/1998 ELI LILLY AND CO PENICILLIN G PROCAINE
13331 I II 9/1/1998 LILLY RESEARCH LABORATORIES ERYTHROMYCIN ESTOLATE
13332 I II 9/1/1998 LILLY RESEARCH LABORATORIES PENICILLIN V POTASSIUM
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  • Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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:

Express Scripts
Dow
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Baxter
McKinsey
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Citi
US Department of Justice

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