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
- 82804-283_917e4926-1e60-473e-9ed8-b9abe08d83f1
- Product NDC
- 82804-283
- Form
- TABLET
- Composition / generic term
- Acetaminophen and Codeine Phosphate
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190910
- 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
- 20 TABLET in 1 BOTTLE (82804-283-20) · 82804-283-20
- 30 TABLET in 1 BOTTLE (82804-283-30) · 82804-283-30
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 →