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
- 17714-012_60f41580-e068-faad-e053-2a91aa0a9076
- Product NDC
- 17714-012
- Form
- TABLET
- Composition / generic term
- Acetaminophen
- Labeler
- Advance Pharmaceutical Inc.
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start / end (source format)
- 19890205
- Source listing expiry
- 20261231
Source-listed ingredients
- ACETAMINOPHEN — 325 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (17714-012-01) · 17714-012-01
- 1000 TABLET in 1 BOTTLE (17714-012-10) · 17714-012-10
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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