NDC 63629-8890 – Oxycodone Hydrochloride

Oxycodone Hydrochloride 30 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC63629-8890

Product details

Brand name
Oxycodone Hydrochloride
Generic name
Oxycodone Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA207418
Marketed since
August 8, 2017
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
63629-8890-130 TABLET in 1 BOTTLE (63629-8890-1)Oct 11, 2021
63629-8890-260 TABLET in 1 BOTTLE (63629-8890-2)Oct 11, 2021
63629-8890-390 TABLET in 1 BOTTLE (63629-8890-3)Oct 11, 2021
63629-8890-4120 TABLET in 1 BOTTLE (63629-8890-4)Oct 11, 2021

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