NDC 71335-1413 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 15 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC71335-1413

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 (9)

Package NDCDescriptionSince
71335-1413-160 TABLET in 1 BOTTLE (71335-1413-1)Feb 3, 2020
71335-1413-290 TABLET in 1 BOTTLE (71335-1413-2)Jul 6, 2020
71335-1413-330 TABLET in 1 BOTTLE (71335-1413-3)Mar 23, 2020
71335-1413-4120 TABLET in 1 BOTTLE (71335-1413-4)Dec 31, 2019
71335-1413-5100 TABLET in 1 BOTTLE (71335-1413-5)Jul 9, 2024
71335-1413-656 TABLET in 1 BOTTLE (71335-1413-6)Jul 9, 2024
71335-1413-784 TABLET in 1 BOTTLE (71335-1413-7)Jul 9, 2024
71335-1413-845 TABLET in 1 BOTTLE (71335-1413-8)Jul 9, 2024
71335-1413-918 TABLET in 1 BOTTLE (71335-1413-9)Jul 9, 2024

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