NDC 71335-0981 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC71335-0981

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 (10)

Package NDCDescriptionSince
71335-0981-015 TABLET in 1 BOTTLE (71335-0981-0)May 30, 2024
71335-0981-130 TABLET in 1 BOTTLE (71335-0981-1)Nov 29, 2018
71335-0981-260 TABLET in 1 BOTTLE (71335-0981-2)Nov 8, 2018
71335-0981-390 TABLET in 1 BOTTLE (71335-0981-3)Nov 30, 2018
71335-0981-456 TABLET in 1 BOTTLE (71335-0981-4)May 30, 2024
71335-0981-5100 TABLET in 1 BOTTLE (71335-0981-5)May 30, 2024
71335-0981-6120 TABLET in 1 BOTTLE (71335-0981-6)May 30, 2024
71335-0981-750 TABLET in 1 BOTTLE (71335-0981-7)May 30, 2024
71335-0981-840 TABLET in 1 BOTTLE (71335-0981-8)May 30, 2024
71335-0981-920 TABLET in 1 BOTTLE (71335-0981-9)Oct 29, 2018

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