Nabumetone

Product NDC
71335-0781
11-digit product format
713350781
Labeler code
71335
Product ID
71335-0781_a7f64f32-2cd0-4e44-b791-430751efe4fc
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nabumentone
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA075280
Marketing category
ANDA
Marketing start
2002-02-25
Marketing end
0000-00-00
Substance
NABUMETONE
Active strength
500 mg/1
Pharmacologic classes
Cyclooxygenase Inhibitors [MoA],Anti-Inflammatory Agents, Non-Steroidal [CS],Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71335-0781-3EA - Each71335-0781737597ff-8f8c-4eb1-a0bd-37fb9f2aa21812022-10-06

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-0781-17133507810120 TABLET in 1 BOTTLE (71335-0781-1) 20 tablet2006-12-280000-00-00NoNoCurrent
71335-0781-27133507810230 TABLET in 1 BOTTLE (71335-0781-2) 30 tablet2006-12-280000-00-00NoNoCurrent
71335-0781-37133507810360 TABLET in 1 BOTTLE (71335-0781-3) 60 tablet2006-12-280000-00-00NoNoCurrent
71335-0781-47133507810490 TABLET in 1 BOTTLE (71335-0781-4) 90 tablet2006-12-280000-00-00NoNoCurrent
71335-0781-57133507810542 TABLET in 1 BOTTLE (71335-0781-5) 42 tablet2006-12-280000-00-00NoNoCurrent
71335-0781-67133507810656 TABLET in 1 BOTTLE (71335-0781-6) 56 tablet2006-12-280000-00-00NoNoCurrent
71335-0781-77133507810714 TABLET in 1 BOTTLE (71335-0781-7) 14 tablet2006-12-280000-00-00NoNoCurrent
71335-0781-871335078108100 TABLET in 1 BOTTLE (71335-0781-8) 100 tablet2006-12-280000-00-00NoNoCurrent
71335-0781-9713350781099 TABLET in 1 BOTTLE (71335-0781-9) 9 tablet2006-12-280000-00-00NoNoCurrent