Tag: generic drugs

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180-Day Exclusivity: How Patent Law Controls Generic Drug Market Entry

The 180-day exclusivity rule lets the first generic drugmaker to challenge a patent block competitors for six months. But delays in launch can extend this monopoly for years-keeping prices high and patients waiting.

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Medicare Part D Formularies: How Generic Coverage Works in 2026

Learn how Medicare Part D covers generic drugs in 2026, including formulary tiers, the $2,000 out-of-pocket cap, cost-saving tips, and how to avoid surprise charges on your prescriptions.

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Generic vs Brand Identification in Pharmacy Systems: Best Practices for Accurate Medication Management

Learn how pharmacy systems accurately identify generic and brand drugs using NDC codes, TE ratings, and FDA guidelines. Best practices for safe substitutions, patient communication, and system setup.

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Bioequivalence for Inhalers, Patches, and Injections: What Generic Drug Developers Really Face

Bioequivalence for inhalers, patches, and injectables requires more than blood tests-it demands matching how the drug is delivered to the body. Learn why these generics are harder to make, why they cost more, and what really makes them work.

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Narrative Medicine: How Personal Stories Shape Acceptance of Generic Medications

Narrative medicine uses patient stories to build trust in generic medications, addressing the emotional barriers that science alone can't fix. It's not about changing the drug-it's about changing the meaning.

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Therapeutic Drug Monitoring: Protecting Patients on Generic NTIs

Therapeutic drug monitoring (TDM) is critical for patients on generic narrow therapeutic index (NTI) drugs, where small changes in blood levels can cause toxicity or treatment failure. Learn when and why TDM saves lives.

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