Oxycodone Hydrochloride

Product NDC
71335-1009
11-digit product format
713351009
Labeler code
71335
Product ID
71335-1009_efeb7bc0-a9bd-4f64-a8a2-f8e323eb3d9b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Oxycodone Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA202662
Marketing category
ANDA
Marketing start
2015-09-22
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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1009-17133510090160 TABLET in 1 BOTTLE (71335-1009-1) 60 tablet2018-11-280000-00-00NoNoCurrent
71335-1009-27133510090290 TABLET in 1 BOTTLE (71335-1009-2) 90 tablet2018-11-280000-00-00NoNoCurrent
71335-1009-37133510090330 TABLET in 1 BOTTLE (71335-1009-3) 30 tablet2018-11-280000-00-00NoNoCurrent
71335-1009-471335100904120 TABLET in 1 BOTTLE (71335-1009-4) 120 tablet2018-11-280000-00-00NoNoCurrent
71335-1009-571335100905100 TABLET in 1 BOTTLE (71335-1009-5) 100 tablet2018-11-280000-00-00NoNoCurrent
71335-1009-67133510090656 TABLET in 1 BOTTLE (71335-1009-6) 56 tablet2018-11-280000-00-00NoNoCurrent
71335-1009-77133510090784 TABLET in 1 BOTTLE (71335-1009-7) 84 tablet2018-11-280000-00-00NoNoCurrent
71335-1009-87133510090845 TABLET in 1 BOTTLE (71335-1009-8) 45 tablet2018-11-280000-00-00NoNoCurrent
71335-1009-97133510090918 TABLET in 1 BOTTLE (71335-1009-9) 18 tablet2018-11-280000-00-00NoNoCurrent