United States · FDA National Drug Code directory

Acetaminophen gelcaps

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: 11673-674_3fea737d-9911-6c9a-e063-6294a90a9664
Product NDC: 11673-674
Form: TABLET
Composition / generic term: Acetaminophen
Labeler: TARGET CORPORATION
Marketing category: OTC MONOGRAPH DRUG
Marketing start / end (source format): 20250710
Source listing expiry: 20271231

Source-listed ingredients

ACETAMINOPHEN — 500 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

1 BOTTLE in 1 CARTON (11673-674-05) / 50 TABLET in 1 BOTTLE · 11673-674-05
225 TABLET in 1 BOTTLE (11673-674-34) · 11673-674-34
1 BOTTLE in 1 CARTON (11673-674-42) / 24 TABLET in 1 BOTTLE · 11673-674-42
100 TABLET in 1 BOTTLE (11673-674-73) · 11673-674-73

Source and coverage

Open FDA National Drug Code directory →

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.

Browse United States records →