Generic Medicines

Quality healthcare at affordable prices


The same active ingredients, same effects, lower cost

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About Generic Medicines

Generic medicines are bioequivalent to brand-name drugs, containing the same active ingredients in the same strength and dosage form.

These medications become available after the patent protection expires on brand-name drugs, typically after 20 years. Generic manufacturers must demonstrate that their product performs identically to the original brand-name drug in terms of safety, efficacy, and quality.

The primary difference between generic and brand-name drugs is the price. Generic medicines are typically 80-85% less expensive than their brand-name counterparts because generic manufacturers don't have to repeat the costly clinical trials of new drugs and generally spend less on marketing.

The grid represents standardization and equivalence

Regulatory Standards for Generic Medicines

Generic medicines must meet rigorous standards to ensure safety and efficacy

Bioequivalence

Must demonstrate equivalent rate and extent of absorption as the brand-name drug.

Quality Standards

Must meet the same stringent quality standards as brand-name medications.

Manufacturing Practices

Produced under the same Good Manufacturing Practices (GMP) as brand-name drugs.

Therapeutic Applications

Generic medicines are available for virtually all therapeutic categories:

Chronic Conditions

Management of hypertension, diabetes, cholesterol, and other long-term health conditions with affordable alternatives.

Infectious Diseases

Antibiotics, antivirals, and antifungals that are equivalent to brand-name treatments at lower costs.

Mental Health

Affordable antidepressants, anxiolytics, and other psychiatric medications that improve accessibility to mental healthcare.

Pain Management

Generic analgesics and anti-inflammatory drugs that provide effective pain relief at lower prices.

Comparison of Medicine Types

Understanding the differences between pharmaceutical approaches

Medicine Type Active Ingredients Cost Regulatory Pathway
Generic Medicines Same as brand-name drugs 80-85% lower than brand-name Abbreviated New Drug Application (ANDA)
Branded Medicines Novel active ingredients Higher due to R&D costs New Drug Application (NDA)
Homeopathic Medicines Highly diluted substances Varies Different regulatory standards

Benefits of Generic Medicines

Cost Savings

Substantially lower prices make medications accessible to more people.

Equivalent Efficacy

Same active ingredients mean the same therapeutic effects as brand-name drugs.

Stringent Regulation

Must meet the same FDA standards for quality, safety, and efficacy.

Increased Access

Lower costs enable more people to afford essential medications.

Healthcare Savings

Reduces overall healthcare costs for individuals and systems.

Market Competition

Multiple manufacturers help keep prices competitive and affordable.

Important Information

While generic medicines contain the same active ingredients as brand-name drugs, they may have different inactive ingredients. If you have allergies or sensitivities to certain ingredients, consult with your healthcare provider or pharmacist. Always inform your healthcare provider about all medications you are taking, including generic versions.