Category: Pharmacy - Page 2

Biosimilar Approval: How the FDA Reviews Biologic Alternatives in 2025

Biosimilar Approval: How the FDA Reviews Biologic Alternatives in 2025

Learn how the FDA's 2025 update to biosimilar approval rules is accelerating access to lower-cost biologic alternatives, why they're not the same as generics, and what this means for patients and providers.

Therapeutic Equivalence Codes: How the FDA Determines If Generic Drugs Can Be Substituted

Therapeutic Equivalence Codes: How the FDA Determines If Generic Drugs Can Be Substituted

The FDA uses therapeutic equivalence codes to determine which generic drugs can safely replace brand-name medications. Learn how A and B codes work, why some generics aren't interchangeable, and how pharmacists use the Orange Book to ensure safe substitutions.

How States Use Incentives to Push Generic Drug Prescribing

How States Use Incentives to Push Generic Drug Prescribing

States use Preferred Drug Lists, pharmacist substitution rules, and copay differences to push generic drug use. These policies save billions without compromising care - but unintended rebate rules are putting some generics at risk.

How to Address Allergies to Inactive Ingredients in Generics

How to Address Allergies to Inactive Ingredients in Generics

Many generic medications contain hidden allergens like lactose, gluten, or food dyes that can trigger reactions-even when the active ingredient is the same as the brand name. Learn how to identify risky excipients and protect yourself.

How to Prevent Moisture Damage to Pills and Capsules: Essential Storage Tips

How to Prevent Moisture Damage to Pills and Capsules: Essential Storage Tips

Learn how to stop moisture from ruining your pills and capsules with simple storage tips, desiccant use, and packaging advice backed by pharmaceutical research. Protect your meds and ensure they work when you need them.

Partial AUC: Advanced Bioequivalence Measurements Explained

Partial AUC: Advanced Bioequivalence Measurements Explained

Partial AUC is a sophisticated pharmacokinetic tool used to assess bioequivalence in complex drug formulations where traditional metrics like Cmax and total AUC fall short. It measures drug exposure during clinically relevant time windows, ensuring generics match brand drugs in both timing and effect.

Mandatory vs Permissive Substitution: How State Laws Control Generic Drug Switching

Mandatory vs Permissive Substitution: How State Laws Control Generic Drug Switching

State laws determine whether pharmacists must or can switch your brand-name prescription to a cheaper generic. These rules affect your costs, safety, and access-and vary widely across the U.S.

Packaging and Labeling: How to Identify Authorized Generics

Packaging and Labeling: How to Identify Authorized Generics

Learn how to identify authorized generics by checking packaging, NDC codes, and labeling. Understand why they're identical to brand drugs but cheaper, and how to confirm you're getting the real thing.

Generic Drug Availability: Why the Same Medicine Costs Different Amounts Around the World

Generic Drug Availability: Why the Same Medicine Costs Different Amounts Around the World

Generic drugs save money-but their availability and price vary wildly around the world. Why do some countries have 80% generic use while others use less than 20%? And why do the same pills cost 10x more in one country than another?

Insurance Coverage of Generic Combinations vs Individual Generics: What You Really Pay

Insurance Coverage of Generic Combinations vs Individual Generics: What You Really Pay

Insurance plans often cover generic combination drugs differently than individual generics, leading to confusing and sometimes costly outcomes. Learn how formularies, tiers, and pricing affect your out-of-pocket costs-and how to save money.

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