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
- 0406-8530_2b25e4bc-e02b-4fd0-a214-1da1b3fb5dd1
- Product NDC
- 0406-8530
- Form
- TABLET
- Composition / generic term
- oxycodone hydrochloride
- Labeler
- SpecGx LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20040630
- 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 (0406-8530-01) · 0406-8530-01
- 1 TABLET in 1 BLISTER PACK (0406-8530-23) · 0406-8530-23
- 100 TABLET in 1 BLISTER PACK (0406-8530-62) · 0406-8530-62
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →