NDC 71335-1023 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 20 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC71335-1023

Product details

Brand name
Oxycodone Hydrochloride
Generic name
Oxycodone
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203638
Marketed since
October 30, 2012
Listing expires
December 31, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (6)

Package NDCDescriptionSince
71335-1023-160 TABLET in 1 BOTTLE (71335-1023-1)Dec 7, 2018
71335-1023-290 TABLET in 1 BOTTLE (71335-1023-2)May 30, 2024
71335-1023-328 TABLET in 1 BOTTLE (71335-1023-3)May 30, 2024
71335-1023-430 TABLET in 1 BOTTLE (71335-1023-4)Feb 25, 2020
71335-1023-58 TABLET in 1 BOTTLE (71335-1023-5)May 30, 2024
71335-1023-66 TABLET in 1 BOTTLE (71335-1023-6)May 30, 2024

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