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U.S. Department of Health and Human Services

Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Search results from the "OB_Rx" table for query on "080354."

Active Ingredient: PREDNISOLONE
Dosage Form;Route: TABLET;ORAL
Proprietary Name: PREDNISOLONE
Applicant: WATSON LABS
Strength: 5MG
Application Number: A080354
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Reference Listed Drug Yes
TE Code:
Patent and Exclusivity Info for this product: View

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FDA/Center for Drug Evaluation and Research
Office of Generic Drugs
Division of Labeling and Program Support
Update Frequency:

Orange Book Data - Monthly
Generic Drug Product Information & Patent Information - Daily
Orange Book Data Updated Through June 2016
Patent and Generic Drug Product Data Last Updated July 22, 2016