There is persistent confusion between generic and branded medicines.

Branded medicines are the original products developed and patented by pharmaceutical companies. They undergo extensive research, clinical trials, and regulatory review.

Generic medicines contain the same active ingredients, dosage form, strength, and intended use as the branded version. Regulatory authorities require generics to demonstrate bioequivalence.

The key difference is price. Generics are typically more affordable because they do not carry the initial research and development costs.

For patients, the decision should be based on medical advice and regulatory approval. In most cases, approved generics are equally safe and effective.