Label: PROPRANOLOL SCOPOLAMINE tablet

  • NDC Code(s): 69267-201-06, 69267-201-12, 69267-201-24, 69267-201-48
  • 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 15, 2014

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

  • INSTRUCTIONS FOR USE

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

    Do not exceed two tablets per day.

  • PRINCIPAL DISPLAY PANEL

    TPS LLCTPS 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

    PROPRANOLOL SCOPOLAMINE TABLET TRITURATE

    20 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

  • INGREDIENTS AND APPEARANCE
    PROPRANOLOL SCOPOLAMINE 
    propranolol scopolamine tablet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:69267-201
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SCOPOLAMINE HYDROBROMIDE (UNII: 451IFR0GXB) (SCOPOLAMINE - UNII:DL48G20X8X) SCOPOLAMINE HYDROBROMIDE.25 mg  in 20.25 mg
    PROPRANOLOL HYDROCHLORIDE (UNII: F8A3652H1V) (PROPRANOLOL - UNII:9Y8NXQ24VQ) PROPRANOLOL HYDROCHLORIDE20 mg  in 20.25 mg
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUND (THE DIAMETER DEPENDS ON DIES) Size5mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69267-201-06121.5 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/01/2014
    2NDC:69267-201-12243 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/01/2014
    3NDC:69267-201-24486 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/01/2014
    4NDC:69267-201-48972 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/01/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other10/01/2014
    Labeler - TPS (044805267)
    Establishment
    NameAddressID/FEIBusiness Operations
    TPS044805267manufacture(69267-201)