United States · FDA National Drug Code directory
Pain Relief
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
- 49580-0821_fc7ae00c-e922-42ff-ba7e-b5f7e7ad14f5
- Product NDC
- 49580-0821
- Form
- SUSPENSION
- Composition / generic term
- Acetaminophen
- Labeler
- P & L Development, LLC
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 20240731
- Source listing expiry
- 20261231
Source-listed ingredients
- ACETAMINOPHEN — 160 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 BOX (49580-0821-4) / 118 mL in 1 BOTTLE, PLASTIC · 49580-0821-4
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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