Tag: ANDA

The FDA uses dissolution testing to ensure generic drugs release their active ingredients at the same rate as brand-name versions. This lab-based method replaces human trials for many drugs, ensuring safety, effectiveness, and consistency without unnecessary costs.

Recent-posts

Olmesartan/Amlodipine Interactions: Essential Guide for Patients and Clinicians

Oct, 23 2025

Recent Drug Safety Communications and Medication Recalls: What You Need to Know

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Specialty Pharmacy: How Providers Manage Generic Specialty Drugs

Jan, 29 2026

Natural Bacterial Vaginosis Remedies: Effectiveness Explained

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Smoking Cessation: Proven Medications and Strategies to Quit for Good

Dec, 26 2025