Label: DANTROLENE SODIUM powder

  • NDC Code(s): 73377-075-01, 73377-075-02, 73377-075-03
  • Packager: AX Pharmaceutical Corp
  • Category: BULK INGREDIENT - ANIMAL DRUG
  • DEA Schedule: None
  • Marketing Status: Bulk Ingredient For Animal Drug Compounding

Drug Label Information

Updated January 3, 2023

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  • Dantrolene Sodium

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  • INGREDIENTS AND APPEARANCE
    DANTROLENE SODIUM 
    dantrolene sodium powder
    Product Information
    Product TypeItem Code (Source)NDC:73377-075
    Route of AdministrationNOT APPLICABLE
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DANTROLENE SODIUM (UNII: 287M0347EV) (DANTROLENE - UNII:F64QU97QCR) DANTROLENE SODIUM1 g  in 1 g
    Product Characteristics
    ColororangeScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73377-075-0150 g in 1 JAR
    2NDC:73377-075-0225000 g in 1 PACKAGE
    3NDC:73377-075-035000 g in 1 PACKAGE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    bulk ingredient for animal drug compounding10/06/2022
    Labeler - AX Pharmaceutical Corp (204011316)
    Establishment
    NameAddressID/FEIBusiness Operations
    AX Pharmaceutical Corp204011316relabel, repack
    Establishment
    NameAddressID/FEIBusiness Operations
    AZICO BIOPHORE INDIA PRIVATE LIMITED860186984api manufacture
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Safety

Report Adverse Events (Animal Drug), FDA Safety Recalls (Animal Drug)

Related Resources

Clinical Trials, PubMed, Biochemical Data Summary

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