United States · FDA National Drug Code directory

Argatroban

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
55150-241_22fd3221-0cbe-4fc2-b4ca-e93faa99b8c0
Product NDC
55150-241
Form
INJECTION, SOLUTION
Composition / generic term
Argatroban
Labeler
Eugia US LLC
Marketing category
NDA
Marketing start / end (source format)
20181127
Source listing expiry
20261231

Source-listed ingredients

  • ARGATROBAN — 50 mg/50mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL, SINGLE-DOSE in 1 CARTON (55150-241-01) / 50 mL in 1 VIAL, SINGLE-DOSE · 55150-241-01
  • 10 VIAL, SINGLE-DOSE in 1 CARTON (55150-241-10) / 50 mL in 1 VIAL, SINGLE-DOSE · 55150-241-10

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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