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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 022311

MOZOBIL (PLERIXAFOR)
24MG/1.2ML (20MG/ML)
Marketing Status: Prescription
Active Ingredient: PLERIXAFOR
Proprietary Name: MOZOBIL
Dosage Form; Route of Administration: SOLUTION; SUBCUTANEOUS
Strength: 24MG/1.2ML (20MG/ML)
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: 
Application Number: N022311
Product Number: 001
Approval Date: Dec 15, 2008
Applicant Holder Full Name: GENZYME CORP
Marketing Status:  Prescription
Patent and Exclusivity Information
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