Generic medicines are pharmaceutical equivalents of brand-name drugs. They contain the same active ingredient in the same strength and dosage form as their brand-name counterparts. The term "generic" simply refers to a medicine that is not protected by a trademark.
| Aspect | Brand Name | Generic |
|---|---|---|
| Active Ingredient | Same | Same |
| Strength | Same | Same |
| Inactive Ingredients | Original formula | May differ slightly |
| Appearance | May be different | Usually different |
| Price | Higher | Lower (30-80% cheaper) |
| Quality Standards | FDA regulated | FDA regulated |
| Efficacy | 100% | Bioequivalent (90-110% of brand) |
YES. The FDA requires that generic medicines be bioequivalent to brand-name drugs. This means:
Extensive clinical testing ensures that generic medicines work exactly like their brand-name equivalents.
Generic medicines undergo the same rigorous safety testing and quality control as brand-name drugs. They must meet the same FDA standards for:
Myth 1: "Generic medicines are made from inferior ingredients"
Reality: Generics contain the same active ingredient. Inactive ingredients may differ but are carefully controlled for safety.
Myth 2: "Generics take longer to work"
Reality: Generics are bioequivalent and work at the same rate as brand-name drugs.
Myth 3: "I can't switch from brand to generic mid-treatment"
Reality: Switching is usually safe, though some patients with seizure disorders may need consultation with their doctor.
Myth 4: "Generics are only for people without insurance"
Reality: Many healthcare professionals and insurance companies recommend generics for all patients seeking cost-effective treatment.