OXYCODONE HYDROCHLORIDE

Product NDC
71335-0174
11-digit product format
713350174
Labeler code
71335
Product ID
71335-0174_cdf8c60b-28ff-4c8d-b9c1-48c59ad0ae0d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
OXYCODONE HYDROCHLORIDE
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA077290
Marketing category
ANDA
Marketing start
2012-12-26
Marketing end
0000-00-00
Substance
OXYCODONE HYDROCHLORIDE
Active strength
15 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA schedule
CII
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
71335-0174-1EA - Each71335-0174249bca7d-83ef-4f56-afa2-04a1acfb4e5312018-04-19

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-0174-17133501740160 TABLET in 1 BOTTLE (71335-0174-1) 60 tablet2015-05-260000-00-00NoNoCurrent
71335-0174-27133501740290 TABLET in 1 BOTTLE (71335-0174-2) 90 tablet2015-05-260000-00-00NoNoCurrent
71335-0174-37133501740330 TABLET in 1 BOTTLE (71335-0174-3) 30 tablet2015-05-260000-00-00NoNoCurrent
71335-0174-471335017404120 TABLET in 1 BOTTLE (71335-0174-4) 120 tablet2015-05-260000-00-00NoNoCurrent
71335-0174-571335017405100 TABLET in 1 BOTTLE (71335-0174-5) 100 tablet2015-05-260000-00-00NoNoCurrent
71335-0174-67133501740656 TABLET in 1 BOTTLE (71335-0174-6) 56 tablet2015-05-260000-00-00NoNoCurrent
71335-0174-77133501740784 TABLET in 1 BOTTLE (71335-0174-7) 84 tablet2015-05-260000-00-00NoNoCurrent
71335-0174-87133501740845 TABLET in 1 BOTTLE (71335-0174-8) 45 tablet2015-05-260000-00-00NoNoCurrent
71335-0174-97133501740918 TABLET in 1 BOTTLE (71335-0174-9) 18 tablet2015-05-260000-00-00NoNoCurrent