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Last Updated: November 22, 2024

Drug Master Files for: phenobarbital sodium


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phenobarbital sodium Drug Master Files

DMF No. Status Type Submission Date Holder Subject
1003 I II 10/19/1966 NYSCO LABS INC PHENOBARBITAL TIMED RELEASE PELLETS
1049 A II 3/21/1967 SIEGFRIED USA LLC PHENOBARBITAL SODIUM USP
1171 I II 4/17/1968 GANES CHEMICALS INC PENNSVILLE DIV G. PACKAGING AND ANALYSIS OF SODIUM PHENOBARBITAL
1322 I 2/12/1969 VICTOR M HERMELIN CO DIV K-V PHARMACAL CO DILAC 30MG /PHENOBARBITAL 45MG SUSTAINED RELEASE CAPSULES
1417 I 9/3/1969 VICTOR M HERMELIN CO DIV K-V PHARMACAL CO DUROTATE PB (PETN 30MG AND PHENOBARBITAL 45MG) SUSTAINED RELEASE CAPS
1603 I II 10/30/1970 GANES CHEMICALS INC PENNSVILLE DIV N,N-DIMETHOXYMETHYLPHENOBARBITAL
>DMF No. >Status >Type >Submission Date >Holder >Subject

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  • Type I Manufacturing Site, Facilities, Operating Procedures, and Personnel (no longer applicable)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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