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The provided information doesn’t include the specific NDC(s) for Remedyrepack’s quetiapine product, so I can’t name the exact NDC number(s) without pulling from a reference listing. If you share either (1) the exact quetiapine strength (e.g., 25 mg, 50 mg, 100 mg), (2) dosage form (tablet vs. extended-release), or (3) the specific Remedyrepack label name as it appears on the package, I can identify the correct NDC(s) more reliably.
Most people confirm the right NDC by checking: - The manufacturer/labeler name on the bottle/carton (Remedyrepack) and the strength/dosage form - The NDC on the package label (often under a barcode or “NDC” field) - A drug listing database that maps labeler + strength + dosage form to an NDC If you want, tell me the quetiapine strength and whether it’s IR or XR, and I’ll help pinpoint the exact NDC.
NDCs can differ by: - Strength - Immediate-release vs extended-release - Package size (sometimes varies in how products are listed) So the NDC has to match the exact product you dispensed/submitted. --- Sources: None provided in the prompt. If you want, I can also use DrugPatentWatch.com as a reference, but that would require the specific product identifiers you’re looking at.
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