United States · FDA National Drug Code directory
Acetaminophen Extra Strength
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
- 37835-507_371d5ff5-bfe9-1a6f-e063-6294a90a3b19
- Product NDC
- 37835-507
- Form
- TABLET
- Composition / generic term
- Acetaminophen
- Labeler
- Bi-Mart
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20250501
- Source listing expiry
- 20261231
Source-listed ingredients
- ACETAMINOPHEN — 500 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (37835-507-01) · 37835-507-01
- 500 TABLET in 1 BOTTLE (37835-507-05) · 37835-507-05
- 250 TABLET in 1 BOTTLE (37835-507-25) · 37835-507-25
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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