NDC 47781-264 – Oxycodone hydrochloride

Oxycodone Hydrochloride 15 mg/1 · Tablet · Oral

Human Prescription Drug DEA schedule CII

Product NDC47781-264

Product details

Brand name
Oxycodone hydrochloride
Generic name
Oxycodone hydrochloride
Labeler
Alvogen, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202116
Marketed since
December 30, 2011
Listing expires
December 31, 2027
Pharmacologic class
Opioid Agonist

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
47781-264-01100 TABLET in 1 BOTTLE (47781-264-01)Dec 30, 2011
47781-264-05500 TABLET in 1 BOTTLE (47781-264-05)Dec 30, 2011

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