Category: Medicines - Page 2

Batch Variability and Bioequivalence: What Acceptable Limits Really Mean for Generic Drugs

Batch-to-batch variability can skew bioequivalence results, leading to false approvals or rejections of generic drugs. Learn how regulators are updating standards to account for real-world manufacturing differences.

Fluoroquinolone Antibiotics and NSAIDs: Why Combining Them Raises Serious Neurologic and Kidney Risks

Combining fluoroquinolone antibiotics with NSAIDs increases the risk of severe kidney injury and neurological damage. Learn why this dangerous interaction happens and what safer alternatives exist.

Modified-Release Formulations: Key Bioequivalence Rules You Need to Know

Modified-release formulations require special bioequivalence testing to ensure generic versions match the brand's release pattern. Learn the key rules, regulatory differences, and why many generics fail.

Stability and Shelf Life: Understanding Generic Drug Degradation and Safety Risks

Understanding how generic drugs degrade over time and why shelf life matters for safety. Learn the science behind stability testing, risks of expired medications, and how storage impacts effectiveness.

Medication Alternatives: What to Do During a Shortage

When medications run out due to shortages, knowing your alternatives can prevent health risks. Learn how to find safe substitutes, work with your pharmacist, and navigate insurance changes during drug shortages in 2026.

Indian Generic Manufacturers: The World's Pharmacy and Global Exports

India supplies 20% of the world's generic medicines and over 60% of global vaccines. Learn how its low-cost, high-quality manufacturing powers global healthcare access.

VA Generic Coverage: How Veterans Affairs Formularies Work in 2026

Learn how the VA formulary works in 2026, including generic drug coverage, tiered copays, Meds by Mail, and how to get your prescriptions approved. Veterans save hundreds annually with VA's low-cost, high-efficiency system.

Bioavailability Studies for Generics: What They Test and Why It Matters for FDA Approval

Bioavailability studies ensure generic drugs are absorbed the same way as brand-name versions. The FDA uses precise pharmacokinetic tests to confirm safety and effectiveness before approval.

Placebo Effect and Generics: How Psychology Affects Generic Medication Success

Many people feel generic medications don’t work as well as brand-name drugs - but the difference is often psychological, not chemical. Learn how expectations shape treatment outcomes and what you can do about it.

How to Read the NDC Number to Confirm the Correct Medication

Learn how to read the NDC number on medication labels to prevent dangerous dispensing errors. Understand the 3-segment code, format conversions, and verification steps used by pharmacies across the U.S.