NDC 71335-0677 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 30 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC71335-0677

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 (8)

Package NDCDescriptionSince
71335-0677-160 TABLET in 1 BOTTLE (71335-0677-1)Mar 9, 2018
71335-0677-290 TABLET in 1 BOTTLE (71335-0677-2)Feb 27, 2018
71335-0677-3120 TABLET in 1 BOTTLE (71335-0677-3)May 24, 2018
71335-0677-430 TABLET in 1 BOTTLE (71335-0677-4)Apr 30, 2018
71335-0677-5100 TABLET in 1 BOTTLE (71335-0677-5)May 29, 2024
71335-0677-640 TABLET in 1 BOTTLE (71335-0677-6)May 29, 2024
71335-0677-718 TABLET in 1 BOTTLE (71335-0677-7)May 29, 2024
71335-0677-828 TABLET in 1 BOTTLE (71335-0677-8)May 29, 2024

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