Tag: FDA generic substitution

Therapeutic Equivalence Codes: How the FDA Determines If Generic Drugs Can Be Substituted

Therapeutic Equivalence Codes: How the FDA Determines If Generic Drugs Can Be Substituted

The FDA uses therapeutic equivalence codes to determine which generic drugs can safely replace brand-name medications. Learn how A and B codes work, why some generics aren't interchangeable, and how pharmacists use the Orange Book to ensure safe substitutions.

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Partial AUC: Advanced Bioequivalence Measurements Explained

Partial AUC is a sophisticated pharmacokinetic tool used to assess bioequivalence in complex drug formulations where traditional metrics like Cmax and total AUC fall short. It measures drug exposure during clinically relevant time windows, ensuring generics match brand drugs in both timing and effect.

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A clear, evidence‑based comparison of Hoodia's oxypregnane, steroidal and glycoside forms versus top weight‑loss alternatives, covering mechanisms, safety, cost, and best‑use tips.

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Sildalis Online Prescription: Your Guide to Sildenafil and Tadalafil Combination Therapy

This article offers an in-depth exploration of Sildalis, a combination therapy of Sildenafil and Tadalafil. It sheds light on the medical benefits, potential side effects, and the recommended dosages of this treatment. Furthermore, it provides guidance on how to safely obtain a Sildalis prescription online, empowering readers with essential knowledge for making informed health decisions.

December 17, 2025
Affirmative Consent Laws: How Patient Permission for Medical Substitution Actually Works

Affirmative consent laws don't apply to medical decisions. Learn how real patient permission works through informed consent and substituted judgment when you can't speak for yourself.