Nadolol

Product NDC
68258-6034
11-digit product format
682586034
Labeler code
68258
Product ID
68258-6034_2990467e-9e2d-4a9d-ba40-64675ae2a5e5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nadolol
Dosage form
TABLET
Route
ORAL
Labeler
Dispensing Solutions, Inc.
Application
ANDA074501
Marketing category
ANDA
Marketing start
2008-10-01
Marketing end
0000-00-00
Substance
NADOLOL
Active strength
40 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
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
c3e14ce3-3dd7-c88b-aff9-2af221ac8a37Product name920240606
8fcb295c-5817-6981-e90d-9999d4e8f347Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68258-6034-32019-11-13C16284748780-197449f38-c179-f6ea-e053-dbdaa90aa703Nadolol Tablets, USP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68258-6034-3Nadolol30 in 1 BOTTLETABLET301

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
NADOLOLACTIVE INGREDIENTFEN504330VNADOLOL TABLET [DISPENSING SOLUTIONS, INC.]1
NADOLOLACTIVE MOIETYFEN504330VNADOLOL TABLET [DISPENSING SOLUTIONS, INC.]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UNADOLOL TABLET [DISPENSING SOLUTIONS, INC.]1
CROSCARMELLOSE SODIUMINACTIVE INGREDIENTM28OL1HH48NADOLOL TABLET [DISPENSING SOLUTIONS, INC.]1
HYDROXYPROPYL CELLULOSEINACTIVE INGREDIENTRFW2ET671PNADOLOL TABLET [DISPENSING SOLUTIONS, INC.]1
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XNADOLOL TABLET [DISPENSING SOLUTIONS, INC.]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30NADOLOL TABLET [DISPENSING SOLUTIONS, INC.]1
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4NADOLOL TABLET [DISPENSING SOLUTIONS, INC.]1
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJNADOLOL TABLET [DISPENSING SOLUTIONS, INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RNADOLOL TABLET [DISPENSING SOLUTIONS, INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68258-6034NADOLOL TABLET [DISPENSING SOLUTIONS, INC.]1Legacy NDC, 1 package rows20120313_d04b1887-933e-4c85-9744-659fe1e56c61.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198007nadolol 40 MG Oral TabletPSNd04b1887-933e-4c85-9744-659fe1e56c611
198007nadolol 40 MG Oral TabletSCDd04b1887-933e-4c85-9744-659fe1e56c611

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
68258-6034-36825860340330 in 1 BOTTLEHistorical