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What “discontinued” usually means for a delavirdine (Rescriptor) FDA label Delavirdine (Rescriptor) was an FDA-approved antiretroviral used for HIV. If you’re seeing that the “label” was discontinued, that typically refers to one of these FDA-status concepts: - The product or marketing authorization is no longer active, so the FDA label page/distribution for that specific version may be removed or marked inactive. - FDA labeling updates may have been superseded or consolidated elsewhere, so the exact “Rescriptor (delavirdine) label” you found is no longer the current labeling document. Why you might see the label marked discontinued Common reasons include: - The manufacturer stopped marketing or discontinued the drug product. - The FDA labeling record was updated or replaced, and the prior label version was retired. - Administrative cleanup on the FDA website when an NDC/product is no longer active. What this means for patients and prescribers - It does not necessarily mean delavirdine is “pulled from safety” by FDA for an acute safety issue. Label discontinuation is often a marketing/record-status change rather than a safety recall. - Clinicians generally rely on the most current FDA labeling (when available) and standard HIV treatment guidance, since antiretroviral regimens are selected based on resistance patterns, comorbidities, interactions, and alternatives. What you should check next To confirm what “label discontinued” means for the exact product you’re looking at, check: - The FDA Drugs@FDA entry for delavirdine/Rescriptor, especially the product status (e.g., whether it’s discontinued, withdrawn, or inactive). - Whether there are newer labeling documents (sometimes the “label discontinued” notice reflects that a document is no longer the current version rather than the drug itself being newly restricted). If you paste the exact wording you’re seeing (or the link/URL and the FDA “Discontinued” date), I can interpret the specific meaning of that label status in context.