PROPRANOLOL SCOPOLAMINE TABLET [TPS]

PROPRANOLOL SCOPOLAMINE TABLET [TPS]
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NDC 69267-202-06, 69267-202-12, 69267-202-24, 69267-202-48
Set ID 05797362-8cc6-35b7-e054-00144ff88e88
Category HUMAN PRESCRIPTION DRUG LABEL
Packager TPS
Generic Name
Product Class Anticholinergic
Product Number
Application Number
  • 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 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

    40 MG/0.5 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

  • INGREDIENTS AND APPEARANCE
    PROPRANOLOL SCOPOLAMINE 
    propranolol scopolamine tablet
    Product Information
    Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:69267-202
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PROPRANOLOL HYDROCHLORIDE (UNII: F8A3652H1V) (PROPRANOLOL - UNII:9Y8NXQ24VQ) PROPRANOLOL HYDROCHLORIDE40 mg  in 40.5 mg
    SCOPOLAMINE HYDROBROMIDE (UNII: 451IFR0GXB) (SCOPOLAMINE - UNII:DL48G20X8X) SCOPOLAMINE HYDROBROMIDE.5 mg  in 40.5 mg
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUND (THE DIAMETER DEPENDS ON DIES) Size5mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69267-202-06243 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/01/2014
    2NDC:69267-202-12486 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/01/2014
    3NDC:69267-202-24972 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/01/2014
    4NDC:69267-202-481944 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(69267-202)

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