Atenolol Scopolamine

Product NDC
69267-101
11-digit product format
692670101
Labeler code
69267
Product ID
69267-101_057842c3-d85b-3282-e054-00144ff88e88
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Atenolol Scopolamine
Dosage form
TABLET
Route
BUCCAL; ORAL; SUBLINGUAL; TRANSMUCOSAL
Labeler
TPS
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2014-10-01
Marketing end
0000-00-00
Substance
ATENOLOL; SCOPOLAMINE HYDROBROMIDE
Active strength
25 mg/25.25mg; mg/25.25mg
Pharmacologic classes
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Anticholinergic [EPC],Cholinergic Antagonists [MoA]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

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#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69267-101-06Atenolol Scopolamine151.5 mg in 1 BOTTLE, PLASTICTABLET151.510
69267-101-12Atenolol Scopolamine303 mg in 1 BOTTLE, PLASTICTABLET30310
69267-101-24Atenolol Scopolamine606 mg in 1 BOTTLE, PLASTICTABLET60610
69267-101-48Atenolol Scopolamine1212 mg in 1 BOTTLE, PLASTICTABLET121210

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ATENOLOLACTIVE INGREDIENT50VV3VW0TIATENOLOL SCOPOLAMINE TABLET [TPS]10
SCOPOLAMINE HYDROBROMIDEACTIVE INGREDIENT451IFR0GXBATENOLOL SCOPOLAMINE TABLET [TPS]10
ATENOLOLACTIVE MOIETY50VV3VW0TIATENOLOL SCOPOLAMINE TABLET [TPS]10
SCOPOLAMINEACTIVE MOIETYDL48G20X8XATENOLOL SCOPOLAMINE TABLET [TPS]10

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69267-101ATENOLOL SCOPOLAMINE TABLET [TPS]10Legacy NDC, 4 package rows20141015_057842c3-d85a-3282-e054-00144ff88e88.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
69267-101-0669267010106151.5 mg in 1 BOTTLE, PLASTIC151.5 mgHistorical
69267-101-1269267010112303 mg in 1 BOTTLE, PLASTIC303 mgHistorical
69267-101-2469267010124606 mg in 1 BOTTLE, PLASTIC606 mgHistorical
69267-101-48692670101481212 mg in 1 BOTTLE, PLASTIC1212 mgHistorical