Label: ATENOLOL SCOPOLAMINE- atenolol scopolamine tablet

  • NDC Code(s): 69267-101-06, 69267-101-12, 69267-101-24, 69267-101-48
  • Packager: TPS
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated October 14, 2014

If you are a consumer or patient please visit this version.

  • INSTRUCTIONS FOR USE

    Take one tablet sublingually or orally as directed by your physician as needed for symptoms of panic or anxiety.

    Do not exceed two tablets per day.

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  • PRINCIPAL DISPLAY PANEL

    TPS LLC

    3524 DECATUR HWY FULTONDALE, AL 35068

    877-608-4995 1-877-608-4995 BT9752747

    Caution: Federal law prohibits transfer of this drug to any other person than patient for whom prescribed

    Rx 263095 Jack Doe/Dr. Jane Doe MD

    JOHN DOE

    123 MAIN ST AUBURN, AL 12345

    ATENOLOL SCOPOLAMINE TABLET TRITURATE

    25 MG/0.25 MG

    48 TABS Lot# Exp

    Take 1 tablet sublingually or orally as directed by your physician as needed for symptoms of panic or anxiety.

    Do not exceed 2 tablets per day

    PH No refills authorized 10/8/2014

    Pill bottle low res.jpg

    TPS LLC

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  • INGREDIENTS AND APPEARANCE
    ATENOLOL SCOPOLAMINE 
    atenolol scopolamine tablet
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:69267-101
    Route of Administration SUBLINGUAL, BUCCAL, TRANSMUCOSAL, ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ATENOLOL (UNII: 50VV3VW0TI) (ATENOLOL - UNII:50VV3VW0TI) ATENOLOL 25 mg  in 25.25 mg
    SCOPOLAMINE HYDROBROMIDE (UNII: 451IFR0GXB) (SCOPOLAMINE - UNII:DL48G20X8X) SCOPOLAMINE HYDROBROMIDE .25 mg  in 25.25 mg
    Product Characteristics
    Color white Score no score
    Shape ROUND (The diameter depends on dies) Size 5mm
    Flavor Imprint Code
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:69267-101-24 606 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/01/2014
    2 NDC:69267-101-06 151.5 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/01/2014
    3 NDC:69267-101-12 303 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/01/2014
    4 NDC:69267-101-48 1212 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 10/01/2014
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 10/01/2014
    Labeler - TPS (044805267)
    Establishment
    Name Address ID/FEI Business Operations
    TPS 044805267 manufacture(69267-101)
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