United States · FDA National Drug Code directory
OXYCODONE AND ACETAMINOPHEN
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
- 0406-0522_5237fd51-c605-4a02-a1ee-c79ddddcb5de
- Product NDC
- 0406-0522
- Form
- TABLET
- Composition / generic term
- oxycodone hydrochloride and acetaminophen
- Labeler
- SpecGx LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20040630
- Source listing expiry
- 20271231
Source-listed ingredients
- OXYCODONE HYDROCHLORIDE — 7.5 mg/1
- ACETAMINOPHEN — 325 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (0406-0522-01) · 0406-0522-01
- 500 TABLET in 1 BOTTLE (0406-0522-05) · 0406-0522-05
- 1 TABLET in 1 BLISTER PACK (0406-0522-23) · 0406-0522-23
- 100 TABLET in 1 BLISTER PACK (0406-0522-62) · 0406-0522-62
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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