Active Ingredient: ARGATROBAN
Proprietary Name: ARGATROBAN IN 0.9% SODIUM CHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INTRAVENOUS
Strength: 250MG/250ML (1MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N206769
Product Number: 001
Approval Date: Dec 15, 2014
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA
Marketing Status:
Discontinued
Patent and Exclusivity Information
