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FDA Approved Drugs·

Approval of Oxybutynin Chloride, Anda #214415 (Labeling)

Approval Date: 01/27/2023; Drug Name: Oxybutynin Chloride, Anda #214415; Active Ingredients: OXYBUTYNIN CHLORIDE; Company: Rubicon; Submission Status: Approval; Submission Classification: Labeling; Application Number: 214415

Company
RUBICON
Keywords
RUBICON