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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 083362

PREDNISOLONE TEBUTATE (PREDNISOLONE TEBUTATE)
20MG/ML
Marketing Status: Discontinued
Active Ingredient: PREDNISOLONE TEBUTATE
Proprietary Name: PREDNISOLONE TEBUTATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: A083362
Product Number: 001
Approval Date: Feb 17, 1984
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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