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
- 0406-0512_5237fd51-c605-4a02-a1ee-c79ddddcb5de
- Product NDC
- 0406-0512
- Form
- TABLET
- Composition / generic term
- oxycodone hydrochloride and acetaminophen
- Labeler
- SpecGx LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19831207
- Source listing expiry
- 20271231
Source-listed ingredients
- OXYCODONE HYDROCHLORIDE — 5 mg/1
- ACETAMINOPHEN — 325 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (0406-0512-01) · 0406-0512-01
- 500 TABLET in 1 BOTTLE (0406-0512-05) · 0406-0512-05
- 1 TABLET in 1 BLISTER PACK (0406-0512-23) · 0406-0512-23
- 100 TABLET in 1 BLISTER PACK (0406-0512-62) · 0406-0512-62
- 5000 TABLET in 1 PAIL (0406-0512-91) · 0406-0512-91
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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