FDA.reportPublic FDA data

Atenolol Scopolamine

Manufacturer
TPS
Effective date
2014-10-15
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-05-31 20:19:37

Label at a glance#

ProductAtenolol Scopolamine
Active ingredientATENOLOL, SCOPOLAMINE HYDROBROMIDE
Label structure2 sections

Label contents#

Full prescribing information#

INSTRUCTIONS FOR USE SECTION

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

Do not exceed two tablets per day.

PACKAGE LABEL.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

50 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

Pill botttle low res.jpgPill botttle low res.jpg

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
ATENOLOL Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813
SCOPOLAMINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fe8ea78e-e1a4-44bf-a6b2-42eed76976bbProduct name520250218
faf41ef3-b4b3-a29e-3b26-07c3009003bfProduct name520220517
5eb1a708-d713-e905-0a08-b103c64796f4Product name320201019

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69267-102-062020-01-31C16284748780-19d75b9d0-659b-f424-e053-dadaa90a57ce05799015-4bf2-4f2a-e054-00144ff88e88
69267-102-122020-01-31C16284748780-19d75b9d0-659b-f424-e053-dadaa90a57ce05799015-4bf2-4f2a-e054-00144ff88e88
69267-102-242020-01-31C16284748780-19d75b9d0-659b-f424-e053-dadaa90a57ce05799015-4bf2-4f2a-e054-00144ff88e88
69267-102-482020-01-31C16284748780-19d75b9d0-659b-f424-e053-dadaa90a57ce05799015-4bf2-4f2a-e054-00144ff88e88

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69267-102-06Atenolol Scopolamine303 mg in 1 BOTTLE, PLASTICTABLET3032
69267-102-12Atenolol Scopolamine606 mg in 1 BOTTLE, PLASTICTABLET6062
69267-102-24Atenolol Scopolamine1212 mg in 1 BOTTLE, PLASTICTABLET12122
69267-102-48Atenolol Scopolamine2424 mg in 1 BOTTLE, PLASTICTABLET24242

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69267-102ATENOLOL SCOPOLAMINE TABLET [TPS]2Legacy NDC, 4 package rows20141015_05799015-4bf2-4f2a-e054-00144ff88e88.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ATENOLOLACTIVE INGREDIENT50VV3VW0TI2
SCOPOLAMINE HYDROBROMIDEACTIVE INGREDIENT451IFR0GXB2
ATENOLOLACTIVE MOIETY50VV3VW0TI2
SCOPOLAMINEACTIVE MOIETYDL48G20X8X2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69267-10269267-102-06, 69267-102-12, 69267-102-24, 69267-102-48

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
ATENOLOL50VV3VW0TIACTIB
SCOPOLAMINE HYDROBROMIDE451IFR0GXBACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
05797362-8cc2-35b7-e054-00144ff88e8805799015-4bf2-4f2a-e054-00144ff88e882014-10-15Exact identifier
spl id: 05797362-8cc2-35b7-e054-00144ff88e88
spl set id: 05799015-4bf2-4f2a-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.