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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 020899

OPTISON (ALBUMIN HUMAN)
10MG/ML
Marketing Status: Prescription
Active Ingredient: ALBUMIN HUMAN
Proprietary Name: OPTISON
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 10MG/ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: 
Application Number: N020899
Product Number: 001
Approval Date: Dec 31, 1997
Applicant Holder Full Name: GE HEALTHCARE
Marketing Status:  Prescription
Patent and Exclusivity Information
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