United States · FDA National Drug Code directory
Aspirin 81 MG
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
- 41250-780_243455d6-158d-31fa-e063-6294a90ad35d
- Product NDC
- 41250-780
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- ASPIRIN
- Labeler
- Meijer
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20110301 / 20261231
Source-listed ingredients
- ASPIRIN — 81 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 PACKAGE (41250-780-01) / 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC · 41250-780-01
- 1 BOTTLE, PLASTIC in 1 PACKAGE (41250-780-06) / 200 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC · 41250-780-06
- 300 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (41250-780-12) · 41250-780-12
- 1 BOTTLE, PLASTIC in 1 PACKAGE (41250-780-14) / 32 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC · 41250-780-14
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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