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
71335-1818_c74c0d98-9483-405c-aab4-06c1cf181074
Product NDC
71335-1818
Form
TABLET
Composition / generic term
acetaminophen and codeine phosphate
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20190802
Source listing expiry
20271231

Source-listed ingredients

  • ACETAMINOPHEN — 300 mg/1
  • CODEINE PHOSPHATE — 30 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 40 TABLET in 1 BOTTLE (71335-1818-0) · 71335-1818-0
  • 6 TABLET in 1 BOTTLE (71335-1818-1) · 71335-1818-1
  • 20 TABLET in 1 BOTTLE (71335-1818-2) · 71335-1818-2
  • 30 TABLET in 1 BOTTLE (71335-1818-3) · 71335-1818-3
  • 84 TABLET in 1 BOTTLE (71335-1818-4) · 71335-1818-4
  • 15 TABLET in 1 BOTTLE (71335-1818-5) · 71335-1818-5
  • 120 TABLET in 1 BOTTLE (71335-1818-6) · 71335-1818-6
  • 100 TABLET in 1 BOTTLE (71335-1818-7) · 71335-1818-7
  • 60 TABLET in 1 BOTTLE (71335-1818-8) · 71335-1818-8
  • 90 TABLET in 1 BOTTLE (71335-1818-9) · 71335-1818-9

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 →