NDC 72162-1337 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 30 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC72162-1337

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 (3)

Package NDCDescriptionSince
72162-1337-330 TABLET in 1 BOTTLE (72162-1337-3)Apr 7, 2026
72162-1337-660 TABLET in 1 BOTTLE (72162-1337-6)Apr 7, 2026
72162-1337-990 TABLET in 1 BOTTLE (72162-1337-9)Apr 7, 2026

Other Oxycodone Hydrochloride products