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
- 55579-110_f49c61bc-9a3e-d885-e053-2995a90ad8af
- Product NDC
- 55579-110
- Form
- INJECTION
- Composition / generic term
- ACETAMINOPHEN
- Labeler
- Solupharm Pharmazeutische Erzeugnisse GmbH
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201207
- Source listing expiry
- 20261231
Source-listed ingredients
- ACETAMINOPHEN — 1000 mg/100mL
These values do not establish equivalence or a dose recommendation.
Packages
- 24 BOTTLE in 1 BOTTLE (55579-110-01) / 100 mL in 1 BOTTLE · 55579-110-01
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 →