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
68083-568_aef05b20-ddc7-48bd-b0b9-8528d15afde9
Product NDC
68083-568
Form
INJECTION, SOLUTION
Composition / generic term
Argatroban
Labeler
Gland Pharma Limited
Marketing category
ANDA
Marketing start / end (source format)
20230731
Source listing expiry
20271231

Source-listed ingredients

  • ARGATROBAN — 50 mg/50mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL in 1 CARTON (68083-568-01) / 50 mL in 1 VIAL · 68083-568-01

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.

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