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
- 67296-0425_530203b1-2a00-c4bc-e063-6294a90a4639
- Product NDC
- 67296-0425
- Form
- TABLET
- Composition / generic term
- oxycodone hydrochloride
- Labeler
- Redpharm Drug
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20040630
- Source listing expiry
- 20271231
Source-listed ingredients
- OXYCODONE HYDROCHLORIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 TABLET in 1 BOTTLE (67296-0425-2) · 67296-0425-2
- 10 TABLET in 1 BOTTLE (67296-0425-3) · 67296-0425-3
- 12 TABLET in 1 BOTTLE (67296-0425-5) · 67296-0425-5
- 40 TABLET in 1 BOTTLE (67296-0425-8) · 67296-0425-8
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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