Oxaprozin

Product NDC
0093-0924
11-digit product format
000930924
Labeler code
0093
Product ID
0093-0924_00bc35bd-6c7b-4259-8b53-cf08f10830f3
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Oxaprozin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Teva Pharmaceuticals USA, Inc.
Application
ANDA075849
Marketing category
ANDA
Marketing start
2003-05-12
Marketing end
0000-00-00
Substance
OXAPROZIN
Active strength
600 mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0093-0924-01EA - Each0093-09240a8411f7-f318-4648-95c8-cf573cf8c2cd12012-07-24
0093-0924-05EA - Each0093-09244c7ec58e-189a-4853-8966-d8067061ed5712012-07-24

DailyMed Socrata Ingredients#

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
312132oxaprozin 600 MG Oral TabletPSNe77d2b9e-84df-4733-b654-16e93618efce1
312132oxaprozin 600 MG Oral TabletSCDe77d2b9e-84df-4733-b654-16e93618efce1
312132oxaprozin 600 MG (as oxaprozin potassium 678 MG) Oral TabletSYe77d2b9e-84df-4733-b654-16e93618efce1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0093-0924-0100093092401100 TABLET, FILM COATED in 1 BOTTLE (0093-0924-01) 2003-05-120000-00-00NoNoCurrent
0093-0924-0500093092405500 TABLET, FILM COATED in 1 BOTTLE (0093-0924-05) 2003-05-120000-00-00NoNoCurrent