NDC 72162-1812 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 30 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC72162-1812

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 (2)

Package NDCDescriptionSince
72162-1812-060 TABLET in 1 BOTTLE (72162-1812-0)May 30, 2024
72162-1812-190 TABLET in 1 BOTTLE (72162-1812-1)May 30, 2024

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