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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for ANDA 211871

Marketing Status: Prescription
Active Ingredient: PODOFILOX
Proprietary Name: PODOFILOX
Dosage Form; Route of Administration: GEL; TOPICAL
Strength: 0.5%
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A211871
Product Number: 001
Approval Date: Nov 22, 2023
Applicant Holder Full Name: PADAGIS US LLC
Marketing Status:  Prescription
Patent and Exclusivity Information
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