NDC 71335-1421 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC71335-1421

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, 2026
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (10)

Package NDCDescriptionSince
71335-1421-015 TABLET in 1 BOTTLE (71335-1421-0)Jul 2, 2024
71335-1421-130 TABLET in 1 BOTTLE (71335-1421-1)Dec 13, 2019
71335-1421-260 TABLET in 1 BOTTLE (71335-1421-2)Dec 16, 2019
71335-1421-390 TABLET in 1 BOTTLE (71335-1421-3)Dec 16, 2019
71335-1421-456 TABLET in 1 BOTTLE (71335-1421-4)Jul 9, 2024
71335-1421-5100 TABLET in 1 BOTTLE (71335-1421-5)Jul 9, 2024
71335-1421-6120 TABLET in 1 BOTTLE (71335-1421-6)Sep 21, 2020
71335-1421-750 TABLET in 1 BOTTLE (71335-1421-7)Jul 9, 2024
71335-1421-840 TABLET in 1 BOTTLE (71335-1421-8)Jul 9, 2024
71335-1421-920 TABLET in 1 BOTTLE (71335-1421-9)Dec 6, 2019

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