Tag: FDA generic drugs

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

Eldepryl (Selegiline) vs Other Parkinson’s Medications: Detailed Comparison

Oct, 17 2025

Professional Liability and Generic Substitution: How Pharmacists Can Reduce Risk

Dec, 18 2025

Timing Medication Doses: How Administration Time Affects Side Effects

Nov, 22 2025

How to Avoid Contamination When Splitting or Crushing Pills: Safe Practices for Home and Care Settings

Nov, 27 2025

Vytorin: Your Guide to Cholesterol Management, Safety, and Results

Jun, 14 2025