Label: ATROPINE SULFATE injection, solution

  • NDC Code(s): 58005-307-04
  • Packager: Sparhawk Laboratories, Inc.
  • Category: PRESCRIPTION ANIMAL DRUG LABEL

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Drug Label Information

Updated February 1, 2017

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  • DESCRIPTION

    INJECTABLE SOLUTION

    FOR ANIMAL USE ONLY

    KEEP OUT OF REACH OF CHILDREN

    CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

    Each mL contains:

    Atropine Sulfate .....................  15 mg
    Sodium Chloride  .....................  9 mg
    Benzyl Alcohol  ..........................  1%
    Water for Injection  ....................  q.s.


  • INDICATIONS:

    For use as an antidote in the treatment of organophosphate insecticide poisoning of cattle, horses and sheep.

  • WARNING:

    Poisonous alkaloid.  Keep out of reach of children.  Antidotes: warmth, emetics, cholinergics

  • STORAGE AND HANDLING

    Store at controlled room temperature between 15o-30oC (59o-86o)

  • DOSAGE AND ADMINISTRATION; INITIAL DOSE:

    Cattle:  20 mg per 100 lbs. of body weight
    Horses:  6.5 mg per 100 lbs. of body weight
    Sheep:  20 mg per 100 lbs. of body weight

    The recommended average initial dose should be split, injecting one quarter (1/4) to one-third (1/3) slowly I.V. and the remainder I.M. or S.C.  After symptoms appear to be under control, repeated maintenance doses should be administered at 3 to 6 hour intervals based on the individual response of the animal.

  • PRINCIPAL DISPLAY PANEL

    Atropine Sulfate LA label

  • INGREDIENTS AND APPEARANCE
    ATROPINE SULFATE 
    atropine sulfate injection, solution
    Product Information
    Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:58005-307
    Route of AdministrationINTRAVENOUS, INTRAMUSCULAR, SUBCUTANEOUS
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ATROPINE SULFATE (UNII: 03J5ZE7KA5) (ATROPINE - UNII:7C0697DR9I) ATROPINE SULFATE 15 mg  in 1 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58005-307-04100 mL in 1 VIAL
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other06/01/1997
    Labeler - Sparhawk Laboratories, Inc. (147979082)