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FDA Approved Drugs·

Approval of Cevimeline Hydrochloride, Anda #216682

Approval Date: 04/06/2023; Drug Name: Cevimeline Hydrochloride, Anda #216682; Active Ingredients: CEVIMELINE HYDROCHLORIDE; Company: Rubicon; Submission Status: Approval; Application Number: 216682

Company
RUBICON
Keywords
RUBICON