NDC 72162-1335 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC72162-1335

Product details

Brand name
Oxycodone Hydrochloride
Generic name
Oxycodone Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA091490
Marketed since
September 8, 2014
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Oxycodone Hydrochloride →

Package NDC codes (4)

Package NDCDescriptionSince
72162-1335-2120 TABLET in 1 BOTTLE (72162-1335-2)Mar 30, 2023
72162-1335-330 TABLET in 1 BOTTLE (72162-1335-3)Mar 30, 2023
72162-1335-660 TABLET in 1 BOTTLE (72162-1335-6)Mar 30, 2023
72162-1335-990 TABLET in 1 BOTTLE (72162-1335-9)Mar 30, 2023

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