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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 022244

LUSEDRA (FOSPROPOFOL DISODIUM)
1050MG/30ML (35MG/ML)
Marketing Status: Discontinued
Active Ingredient: FOSPROPOFOL DISODIUM
Proprietary Name: LUSEDRA
Dosage Form; Route of Administration: SOLUTION; INTRAVENOUS
Strength: 1050MG/30ML (35MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N022244
Product Number: 001
Approval Date: Dec 12, 2008
Applicant Holder Full Name: EISAI INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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