NDC 72162-1336 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 15 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC72162-1336

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 (1)

Package NDCDescriptionSince
72162-1336-1100 TABLET in 1 BOTTLE, PLASTIC (72162-1336-1)Apr 7, 2026

Other Oxycodone Hydrochloride products