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
- 47781-264_aa023689-6275-e0a0-ab08-d45edc45ec40
- Product NDC
- 47781-264
- 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 — 15 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (47781-264-01) · 47781-264-01
- 500 TABLET in 1 BOTTLE (47781-264-05) · 47781-264-05
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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