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
- 87063-033_44677216-216d-f82c-e063-6294a90a3dca
- Product NDC
- 87063-033
- Form
- TABLET
- Composition / generic term
- oxycodone and acetaminophen
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190601
- Source listing expiry
- 20261231
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 (87063-033-01) · 87063-033-01
- 500 TABLET in 1 BOTTLE (87063-033-05) · 87063-033-05
- 10 TABLET in 1 BOTTLE (87063-033-10) · 87063-033-10
- 20 TABLET in 1 BOTTLE (87063-033-20) · 87063-033-20
- 30 TABLET in 1 BOTTLE (87063-033-30) · 87063-033-30
- 60 TABLET in 1 BOTTLE (87063-033-60) · 87063-033-60
- 90 TABLET in 1 BOTTLE (87063-033-90) · 87063-033-90
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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