Oxycodone and Acetaminophen

Product NDC
71335-0193
11-digit product format
713350193
Labeler code
71335
Product ID
71335-0193_c934f2d4-55e1-4deb-aa12-9b246a620b9e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Oxycodone and Acetaminophen
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA040777
Marketing category
ANDA
Marketing start
2007-11-27
Marketing end
0000-00-00
Substance
ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE
Active strength
325 mg/1; mg/1
Pharmacologic classes
Full Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA schedule
CII
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-0193-07133501930025 TABLET in 1 BOTTLE (71335-0193-0) 25 tablet2007-11-270000-00-00NoNoCurrent
71335-0193-17133501930110 TABLET in 1 BOTTLE (71335-0193-1) 10 tablet2007-11-270000-00-00NoNoCurrent
71335-0193-271335019302120 TABLET in 1 BOTTLE (71335-0193-2) 120 tablet2007-11-270000-00-00NoNoCurrent
71335-0193-37133501930328 TABLET in 1 BOTTLE (71335-0193-3) 28 tablet2007-11-270000-00-00NoNoCurrent
71335-0193-47133501930412 TABLET in 1 BOTTLE (71335-0193-4) 12 tablet2007-11-270000-00-00NoNoCurrent
71335-0193-57133501930540 TABLET in 1 BOTTLE (71335-0193-5) 40 tablet2007-11-270000-00-00NoNoCurrent
71335-0193-67133501930630 TABLET in 1 BOTTLE (71335-0193-6) 30 tablet2007-11-270000-00-00NoNoCurrent
71335-0193-77133501930790 TABLET in 1 BOTTLE (71335-0193-7) 90 tablet2007-11-270000-00-00NoNoCurrent
71335-0193-87133501930860 TABLET in 1 BOTTLE (71335-0193-8) 60 tablet2007-11-270000-00-00NoNoCurrent
71335-0193-97133501930984 TABLET in 1 BOTTLE (71335-0193-9) 84 tablet2007-11-270000-00-00NoNoCurrent