United States · FDA National Drug Code directory

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
55289-880_48390181-cda8-a543-e063-6294a90a5896
Product NDC
55289-880
Form
TABLET
Composition / generic term
Acetaminophen
Labeler
PD-Rx Pharmaceuticals, Inc.
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20060110
Source listing expiry
20271231

Source-listed ingredients

  • ACETAMINOPHEN — 500 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE, PLASTIC (55289-880-01) · 55289-880-01
  • 6 TABLET in 1 BOTTLE, PLASTIC (55289-880-06) · 55289-880-06
  • 12 TABLET in 1 BOTTLE, PLASTIC (55289-880-12) · 55289-880-12
  • 20 TABLET in 1 BOTTLE, PLASTIC (55289-880-20) · 55289-880-20
  • 21 TABLET in 1 BOTTLE, PLASTIC (55289-880-21) · 55289-880-21
  • 24 TABLET in 1 BOTTLE, PLASTIC (55289-880-24) · 55289-880-24
  • 30 TABLET in 1 BOTTLE, PLASTIC (55289-880-30) · 55289-880-30
  • 50 TABLET in 1 BOTTLE, PLASTIC (55289-880-50) · 55289-880-50
  • 60 TABLET in 1 BOTTLE, PLASTIC (55289-880-60) · 55289-880-60
  • 200 TABLET in 1 BOTTLE, PLASTIC (55289-880-97) · 55289-880-97

Source and coverage

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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.

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