NDC 71335-1080 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 15 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC71335-1080

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 (9)

Package NDCDescriptionSince
71335-1080-160 TABLET in 1 BOTTLE (71335-1080-1)Jan 29, 2019
71335-1080-290 TABLET in 1 BOTTLE (71335-1080-2)Jan 29, 2019
71335-1080-330 TABLET in 1 BOTTLE (71335-1080-3)Feb 15, 2019
71335-1080-4120 TABLET in 1 BOTTLE (71335-1080-4)May 7, 2019
71335-1080-5100 TABLET in 1 BOTTLE (71335-1080-5)May 30, 2024
71335-1080-656 TABLET in 1 BOTTLE (71335-1080-6)May 30, 2024
71335-1080-784 TABLET in 1 BOTTLE (71335-1080-7)May 30, 2024
71335-1080-845 TABLET in 1 BOTTLE (71335-1080-8)May 30, 2024
71335-1080-918 TABLET in 1 BOTTLE (71335-1080-9)May 30, 2024

Other Oxycodone Hydrochloride products