United States · FDA National Drug Code directory

Acetaminophen and Codeine Phosphate

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
71335-0336_dd27c850-8f70-4492-9a8c-9610b5ff58d2
Product NDC
71335-0336
Form
TABLET
Composition / generic term
Acetaminophen and Codeine Phosphate
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20130415
Source listing expiry
20261231

Source-listed ingredients

  • ACETAMINOPHEN — 300 mg/1
  • CODEINE PHOSPHATE — 60 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (71335-0336-0) · 71335-0336-0
  • 30 TABLET in 1 BOTTLE (71335-0336-1) · 71335-0336-1
  • 120 TABLET in 1 BOTTLE (71335-0336-2) · 71335-0336-2
  • 60 TABLET in 1 BOTTLE (71335-0336-3) · 71335-0336-3
  • 90 TABLET in 1 BOTTLE (71335-0336-4) · 71335-0336-4
  • 40 TABLET in 1 BOTTLE (71335-0336-5) · 71335-0336-5
  • 20 TABLET in 1 BOTTLE (71335-0336-6) · 71335-0336-6
  • 112 TABLET in 1 BOTTLE (71335-0336-7) · 71335-0336-7
  • 84 TABLET in 1 BOTTLE (71335-0336-8) · 71335-0336-8
  • 15 TABLET in 1 BOTTLE (71335-0336-9) · 71335-0336-9

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 →