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
- 76420-362_46f094b6-4d19-8b98-e063-6294a90a5aac
- Product NDC
- 76420-362
- Form
- TABLET
- Composition / generic term
- Oxycodone Hydrochloride
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240910
- Source listing expiry
- 20261231
Source-listed ingredients
- OXYCODONE HYDROCHLORIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE, PLASTIC (76420-362-01) · 76420-362-01
- 500 TABLET in 1 BOTTLE, PLASTIC (76420-362-05) · 76420-362-05
- 10 TABLET in 1 BOTTLE, PLASTIC (76420-362-10) · 76420-362-10
- 30 TABLET in 1 BOTTLE, PLASTIC (76420-362-30) · 76420-362-30
- 60 TABLET in 1 BOTTLE, PLASTIC (76420-362-60) · 76420-362-60
- 90 TABLET in 1 BOTTLE, PLASTIC (76420-362-90) · 76420-362-90
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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