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
71335-1472_2a24bfb7-1612-4af3-86c4-7664ba56db9e
Product NDC
71335-1472
Form
TABLET
Composition / generic term
Oxycodone and Acetaminophen
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20140828
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

  • 84 TABLET in 1 BOTTLE (71335-1472-0) · 71335-1472-0
  • 120 TABLET in 1 BOTTLE (71335-1472-1) · 71335-1472-1
  • 90 TABLET in 1 BOTTLE (71335-1472-2) · 71335-1472-2
  • 60 TABLET in 1 BOTTLE, PLASTIC (71335-1472-3) · 71335-1472-3
  • 30 TABLET in 1 BOTTLE (71335-1472-4) · 71335-1472-4
  • 100 TABLET in 1 BOTTLE (71335-1472-5) · 71335-1472-5
  • 45 TABLET in 1 BOTTLE (71335-1472-6) · 71335-1472-6
  • 28 TABLET in 1 BOTTLE (71335-1472-7) · 71335-1472-7
  • 168 TABLET in 1 BOTTLE (71335-1472-8) · 71335-1472-8
  • 20 TABLET in 1 BOTTLE (71335-1472-9) · 71335-1472-9

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 →