FDA.reportPublic FDA data

Nadolol

Product NDC
0093-4235
11-digit product format
000934235
Labeler code
0093
Product ID
0093-4235_af5152c5-3641-4622-9295-02e9ac51b0d5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nadolol
Dosage form
TABLET
Route
ORAL
Labeler
Teva Pharmaceuticals USA, Inc.
Application
ANDA074229
Marketing category
ANDA
Marketing start
2008-11-03
Marketing end
0000-00-00
Substance
NADOLOL
Active strength
20 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0093-4235-01EA - Each0093-4235ad0e8b3b-3447-4323-866d-b42ae094e79312012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
NadololACTIVE INGREDIENTFEN504330VNADOLOL TABLET [REBEL DISTRIBUTORS CORP]1
NadololACTIVE MOIETYFEN504330VNADOLOL TABLET [REBEL DISTRIBUTORS CORP]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UNADOLOL TABLET [REBEL DISTRIBUTORS CORP]1
CITRIC ACID MONOHYDRATEINACTIVE INGREDIENT2968PHW8QPNADOLOL TABLET [REBEL DISTRIBUTORS CORP]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30NADOLOL TABLET [REBEL DISTRIBUTORS CORP]1
POVIDONEINACTIVE INGREDIENTFZ989GH94ENADOLOL TABLET [REBEL DISTRIBUTORS CORP]1
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJNADOLOL TABLET [REBEL DISTRIBUTORS CORP]1

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
198006nadolol 20 MG Oral TabletPSN0c6eed96-edfd-4e65-8eff-59d1ad51a59a1
198006nadolol 20 MG Oral TabletSCD0c6eed96-edfd-4e65-8eff-59d1ad51a59a1