NDC 65162-047 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 5 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC65162-047

Product details

Brand name
Oxycodone Hydrochloride
Generic name
Oxycodone
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203638
Marketed since
October 30, 2012
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

Uses, dosage, side effects and warnings for Oxycodone Hydrochloride →

Package NDC codes (4)

Package NDCDescriptionSince
65162-047-0330 TABLET in 1 BOTTLE (65162-047-03)Oct 30, 2012
65162-047-10100 TABLET in 1 BOTTLE (65162-047-10)Oct 30, 2012
65162-047-25250 TABLET in 1 BOTTLE (65162-047-25)Oct 30, 2012
65162-047-50500 TABLET in 1 BOTTLE (65162-047-50)Oct 30, 2012

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