Oxycodone Hydrochloride

Product NDC
71335-2816
11-digit product format
713352816
Labeler code
71335
Product ID
71335-2816_0e4c01bc-f352-4907-bd04-a4ff95cfdcab
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Oxycodone Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA077712
Marketing category
ANDA
Marketing start
2024-09-10
Substance
OXYCODONE HYDROCHLORIDE
Active strength
30 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA], Opioid Agonist [EPC]
DEA schedule
CII
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
C1ENJ2TE6COXYCODONE HYDROCHLORIDE124-90-3OXYCODONE HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-2816-17133528160160 TABLET in 1 BOTTLE, PLASTIC (71335-2816-1) 60 tablet2025-10-16NoNoHistorical
71335-2816-27133528160290 TABLET in 1 BOTTLE, PLASTIC (71335-2816-2) 90 tablet2025-10-16NoNoHistorical
71335-2816-371335281603120 TABLET in 1 BOTTLE, PLASTIC (71335-2816-3) 120 tablet2025-10-16NoNoHistorical
71335-2816-47133528160430 TABLET in 1 BOTTLE, PLASTIC (71335-2816-4) 30 tablet2025-10-16NoNoHistorical
71335-2816-571335281605100 TABLET in 1 BOTTLE, PLASTIC (71335-2816-5) 100 tablet2025-10-16NoNoHistorical
71335-2816-67133528160640 TABLET in 1 BOTTLE, PLASTIC (71335-2816-6) 40 tablet2025-10-16NoNoHistorical
71335-2816-77133528160718 TABLET in 1 BOTTLE, PLASTIC (71335-2816-7) 18 tablet2025-10-16NoNoHistorical
71335-2816-87133528160828 TABLET in 1 BOTTLE, PLASTIC (71335-2816-8) 28 tablet2025-10-16NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Oxycodone HydrochlorideBryant Ranch Prepack2025-10-16HUMAN PRESCRIPTION DRUG LABEL1