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Generated: March 23, 2019

DrugPatentWatch Database Preview

Drug Master Files for: Beecham

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Beecham Drug Master Files

DMF No. Status Type Submission Date Holder Subject
10266 I II 6/3/1993 SMITHKLINE BEECHAM PHARMACEUTICALS BRL 47539 (2-ACETOXYMETHYL-4-IODOBUT-1-YL-ACETATE)
10267 I II 6/3/1993 SMITHKLINE BEECHAM PHARMACEUTICALS BRL 47539 (2-ACETOXYMETHYL-4-IODOBUT-1-YL-ACETATE)
11041 I II 6/24/1994 SMITHKLINE BEECHAM PHARMACEUTICALS CO PENICILLIN G POTASSIUM, NON-STERILE, TECHNICAL GRADE
11400 I II 3/24/1995 SMITHKLINE BEECHAM PHARMACEUTICALS MANUFACTURING SITE, FACILITIES, PERSONNEL, AND GENERAL OPERATING PROCEDURES IN CUERNAVACA, MEXICO.
11805 I II 1/11/1996 SMITHKLINE BEECHAM PHARMACEUTICALS CIMETIDINE
12933 I II 3/31/1998 SMITHKLINE BEECHAM 6-AMINOPENICILLANIC ACID [6-APA]
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  • Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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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