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
- 71335-9674_33818371-4f87-41f2-ac3d-4ec756d79131
- Product NDC
- 71335-9674
- Form
- TABLET
- Composition / generic term
- oxycodone and acetaminophen
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190601
- 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
- 25 TABLET in 1 BOTTLE (71335-9674-0) · 71335-9674-0
- 10 TABLET in 1 BOTTLE (71335-9674-1) · 71335-9674-1
- 120 TABLET in 1 BOTTLE (71335-9674-2) · 71335-9674-2
- 28 TABLET in 1 BOTTLE (71335-9674-3) · 71335-9674-3
- 12 TABLET in 1 BOTTLE (71335-9674-4) · 71335-9674-4
- 40 TABLET in 1 BOTTLE (71335-9674-5) · 71335-9674-5
- 30 TABLET in 1 BOTTLE (71335-9674-6) · 71335-9674-6
- 90 TABLET in 1 BOTTLE (71335-9674-7) · 71335-9674-7
- 60 TABLET in 1 BOTTLE (71335-9674-8) · 71335-9674-8
- 84 TABLET in 1 BOTTLE (71335-9674-9) · 71335-9674-9
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 →