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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 019157

PEDIAPRED (PREDNISOLONE SODIUM PHOSPHATE)
EQ 5MG BASE/5ML
Marketing Status: Prescription
Active Ingredient: PREDNISOLONE SODIUM PHOSPHATE
Proprietary Name: PEDIAPRED
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: EQ 5MG BASE/5ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AA
Application Number: N019157
Product Number: 001
Approval Date: May 28, 1986
Applicant Holder Full Name: SETON PHARMACEUTICAL LLC
Marketing Status:  Prescription
Patent and Exclusivity Information
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