NDC 71335-1361 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC71335-1361

Product details

Brand name
Oxycodone Hydrochloride
Generic name
Oxycodone Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202160
Marketed since
July 12, 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
71335-1361-015 TABLET in 1 BOTTLE (71335-1361-0)Aug 12, 2024
71335-1361-130 TABLET in 1 BOTTLE (71335-1361-1)Nov 19, 2019
71335-1361-260 TABLET in 1 BOTTLE (71335-1361-2)Oct 1, 2019
71335-1361-390 TABLET in 1 BOTTLE (71335-1361-3)Oct 1, 2019
71335-1361-456 TABLET in 1 BOTTLE (71335-1361-4)Aug 12, 2024
71335-1361-5100 TABLET in 1 BOTTLE (71335-1361-5)Aug 12, 2024
71335-1361-6120 TABLET in 1 BOTTLE (71335-1361-6)Aug 12, 2024
71335-1361-750 TABLET in 1 BOTTLE (71335-1361-7)Aug 12, 2024
71335-1361-840 TABLET in 1 BOTTLE (71335-1361-8)Aug 12, 2024
71335-1361-920 TABLET in 1 BOTTLE (71335-1361-9)Oct 18, 2019

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