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FDA Approved Drugs·

Approval of Nortriptyline Hydrochloride, Anda #217731

Approval Date: 08/15/2023; Drug Name: Nortriptyline Hydrochloride, Anda #217731; Active Ingredients: NORTRIPTYLINE HYDROCHLORIDE; Company: Rubicon; Submission Status: Approval; Application Number: 217731

Company
RUBICON
Keywords
RUBICON