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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 089521

Marketing Status: Discontinued
Active Ingredient: PHENYTOIN SODIUM
Proprietary Name: PHENYTOIN SODIUM
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 50MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A089521
Product Number: 001
Approval Date: Mar 17, 1987
Applicant Holder Full Name: HOSPIRA INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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