Oxaprozin

Product NDC
66336-722
11-digit product format
663360722
Labeler code
66336
Product ID
66336-722_07a2440f-fa26-4502-bd79-f4c6d1942c8c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Oxaprozin
Dosage form
TABLET
Route
ORAL
Labeler
Dispensing Solutions, Inc.
Application
ANDA075845
Marketing category
ANDA
Marketing start
2001-01-31
Marketing end
0000-00-00
Substance
OXAPROZIN
Active strength
600 mg/1
Pharmacologic classes
Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [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
95b4bbb5-24e2-44a4-b351-d64e35d6e76aProduct name120250722
486cfca4-efa2-1446-eef2-3c74b667bb18Product name220170713

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
66336-722-602019-11-27C16284748780-19855d018-ea44-cd31-e053-dbdaa90ab51aOxaprozin Tablets USP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
66336-722-60Oxaprozin60 in 1 BOTTLETABLET601

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
66336-722-60EA - Each66336-7227d368ea0-cc6c-4188-8c87-ea024b075a5a12013-08-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
OXAPROZINACTIVE INGREDIENTMHJ80W9LRBOXAPROZIN TABLET [DISPENSING SOLUTIONS, INC.]1
OXAPROZINACTIVE MOIETYMHJ80W9LRBOXAPROZIN TABLET [DISPENSING SOLUTIONS, INC.]1
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UOXAPROZIN TABLET [DISPENSING SOLUTIONS, INC.]1
HYPROMELLOSESINACTIVE INGREDIENT3NXW29V3WOOXAPROZIN TABLET [DISPENSING SOLUTIONS, INC.]1
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30OXAPROZIN TABLET [DISPENSING SOLUTIONS, INC.]1
METHYLCELLULOSE (100 CPS)INACTIVE INGREDIENT4GFU244C4JOXAPROZIN TABLET [DISPENSING SOLUTIONS, INC.]1
POLACRILIN POTASSIUMINACTIVE INGREDIENT0BZ5A00FQUOXAPROZIN TABLET [DISPENSING SOLUTIONS, INC.]1
POLYETHYLENE GLYCOLSINACTIVE INGREDIENT3WJQ0SDW1AOXAPROZIN TABLET [DISPENSING SOLUTIONS, INC.]1
POLYSORBATE 80INACTIVE INGREDIENT6OZP39ZG8HOXAPROZIN TABLET [DISPENSING SOLUTIONS, INC.]1
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4OXAPROZIN TABLET [DISPENSING SOLUTIONS, INC.]1
STARCH, CORNINACTIVE INGREDIENTO8232NY3SJOXAPROZIN TABLET [DISPENSING SOLUTIONS, INC.]1
TITANIUM DIOXIDEINACTIVE INGREDIENT15FIX9V2JPOXAPROZIN TABLET [DISPENSING SOLUTIONS, INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66336-722OXAPROZIN TABLET [DISPENSING SOLUTIONS, INC.]1Legacy NDC, 1 package rows20130704_73328d94-587c-4518-8856-98e297124665.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
312132oxaprozin 600 MG Oral TabletPSN73328d94-587c-4518-8856-98e2971246651
312132oxaprozin 600 MG Oral TabletSCD73328d94-587c-4518-8856-98e2971246651
312132oxaprozin 600 MG (as oxaprozin potassium 678 MG) Oral TabletSY73328d94-587c-4518-8856-98e2971246651

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
66336-722-606633607226060 in 1 BOTTLEHistorical