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
- 70038-131_4652d772-fe08-2ce4-e063-6294a90a1ddd
- Product NDC
- 70038-131
- Form
- TABLET
- Composition / generic term
- Acetaminophen
- Labeler
- RAONBIO CORP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20240101
- Source listing expiry
- 20261231
Source-listed ingredients
- ACETAMINOPHEN — 250 mg/1
- IBUPROFEN — 125 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 36 TABLET in 1 BOTTLE (70038-131-36) · 70038-131-36
- 72 TABLET in 1 BOTTLE (70038-131-72) · 70038-131-72
- 18 TABLET in 1 BOTTLE (70038-131-81) · 70038-131-81
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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