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
- 71205-329_12b8ef8f-90ab-4366-9a82-e6164926eb84
- Product NDC
- 71205-329
- Form
- TABLET
- Composition / generic term
- Oxycodone and Acetaminophen
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170411
- Source listing expiry
- 20261231
Source-listed ingredients
- OXYCODONE HYDROCHLORIDE — 5 mg/1
- ACETAMINOPHEN — 325 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET in 1 BOTTLE (71205-329-10) · 71205-329-10
- 28 TABLET in 1 BOTTLE (71205-329-28) · 71205-329-28
- 30 TABLET in 1 BOTTLE (71205-329-30) · 71205-329-30
- 60 TABLET in 1 BOTTLE (71205-329-60) · 71205-329-60
- 90 TABLET in 1 BOTTLE (71205-329-90) · 71205-329-90
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 →