United States · FDA National Drug Code directory

Oxycodone hydrochloride

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 47781-265_aa023689-6275-e0a0-ab08-d45edc45ec40
Product NDC: 47781-265
Form: TABLET
Composition / generic term: Oxycodone hydrochloride
Labeler: Alvogen, Inc.
Marketing category: ANDA
Marketing start / end (source format): 20111230
Source listing expiry: 20271231

Source-listed ingredients

OXYCODONE HYDROCHLORIDE — 30 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 TABLET in 1 BOTTLE (47781-265-01) · 47781-265-01
500 TABLET in 1 BOTTLE (47781-265-05) · 47781-265-05

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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