Oxaprozin

Product NDC
71335-0902
11-digit product format
713350902
Labeler code
71335
Product ID
71335-0902_0ab53651-f4c8-4aa7-9669-a09bd0a81cc5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Oxaprozin
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA075845
Marketing category
ANDA
Marketing start
2001-01-31
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 Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71335-0902OXAPROZIN TABLET [BRYANT RANCH PREPACK]7Legacy NDC20240830_0ab53651-f4c8-4aa7-9669-a09bd0a81cc5.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-0902-17133509020130 TABLET in 1 BOTTLE (71335-0902-1) 30 tablet2021-12-270000-00-00NoNoCurrent
71335-0902-27133509020220 TABLET in 1 BOTTLE (71335-0902-2) 20 tablet2021-12-270000-00-00NoNoCurrent
71335-0902-37133509020314 TABLET in 1 BOTTLE (71335-0902-3) 14 tablet2021-12-270000-00-00NoNoCurrent
71335-0902-47133509020460 TABLET in 1 BOTTLE (71335-0902-4) 60 tablet2018-07-110000-00-00NoNoCurrent
71335-0902-57133509020590 TABLET in 1 BOTTLE (71335-0902-5) 90 tablet2021-12-270000-00-00NoNoCurrent
71335-0902-6713350902066 TABLET in 1 BOTTLE (71335-0902-6) 6 tablet2021-12-270000-00-00NoNoCurrent
71335-0902-771335090207120 TABLET in 1 BOTTLE (71335-0902-7) 120 tablet2021-12-270000-00-00NoNoCurrent