What are Doptelet (avatrombopag) FDA NDC codes that are active vs. inactive?
I don’t have enough information in the provided prompt to list Doptelet’s specific FDA NDC codes and their active/inactive status. NDC availability changes by package size, manufacturer/labeler, and can vary over time.
If you share either:
- the exact Doptelet dosage form/strength (e.g., 20 mg tablets, etc.), and/or
- the labeler/manufacturer you see on the product (from the bottle or prescription),
I can help you map that to the correct active/inactive NDC entry once you provide the relevant NDC lookup results or the dataset you’re using.
Where to check the official active vs. inactive NDC status
For authoritative active/inactive status, the usual sources are:
- the FDA NDC Directory (official registry of NDCs and labeler/product details)
- your pharmacy’s NDC database (often mirrors FDA data but can lag)
- wholesaler/pharmacy packaging listings (may show “inactive” once stock is discontinued, which is not the same as FDA directory status)
What I need from you to produce the exact active/inactive list
Reply with one of the following, and I’ll format the result clearly:
1) The NDC Directory export/table you’re using (paste rows for “Doptelet” or “avatrombopag”), or
2) The specific NDC(s) you want checked (paste the numbers), or
3) The exact product identifiers you’re looking for (strength + package type), and the labeler name shown.
Sources are required to give exact codes and statuses, and none are included in your prompt.