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
- 71399-1026_59d1ee76-55a2-f982-e063-6294a90af0a1
- Product NDC
- 71399-1026
- Form
- TABLET
- Composition / generic term
- Acetaminophen
- Labeler
- Akron Pharma Inc.
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20241206
- 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 (71399-1026-1) · 71399-1026-1
- 1000 TABLET in 1 BOTTLE (71399-1026-2) · 71399-1026-2
- 24 TABLET in 1 BOTTLE (71399-1026-4) · 71399-1026-4
- 500 TABLET in 1 BOTTLE (71399-1026-5) · 71399-1026-5
- 50 TABLET in 1 BOTTLE (71399-1026-6) · 71399-1026-6
- 100000 TABLET in 1 DRUM (71399-1026-8) · 71399-1026-8
- 60000 TABLET in 1 DRUM (71399-1026-9) · 71399-1026-9
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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