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
- 71335-1522_71cd2ab2-dbe2-4c8b-904a-c8ad320181f9
- Product NDC
- 71335-1522
- Form
- TABLET
- Composition / generic term
- acetaminophen and codeine phosphate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20010531
- Source listing expiry
- 20261231
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 (71335-1522-0) · 71335-1522-0
- 6 TABLET in 1 BOTTLE (71335-1522-1) · 71335-1522-1
- 20 TABLET in 1 BOTTLE (71335-1522-2) · 71335-1522-2
- 30 TABLET in 1 BOTTLE (71335-1522-3) · 71335-1522-3
- 84 TABLET in 1 BOTTLE (71335-1522-4) · 71335-1522-4
- 15 TABLET in 1 BOTTLE (71335-1522-5) · 71335-1522-5
- 120 TABLET in 1 BOTTLE (71335-1522-6) · 71335-1522-6
- 100 TABLET in 1 BOTTLE (71335-1522-7) · 71335-1522-7
- 60 TABLET in 1 BOTTLE (71335-1522-8) · 71335-1522-8
- 90 TABLET in 1 BOTTLE (71335-1522-9) · 71335-1522-9
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 →