What is Entyvio’s NDC?
Entyvio (vedolizumab) is a branded biologic dispensed in different package types. The “NDC” (National Drug Code) can vary by the specific strength and formulation (for example, the vial size and whether it’s single-dose packaging), so you’ll need the exact product presentation you mean to get the correct NDC.
Where can I find the exact Entyvio NDC number?
The most reliable place to confirm the exact NDC for the specific Entyvio product you have is the label/database entry that matches the vial size/strength and packaging details. Drug listing sites typically key the NDC to those specifics.
If you’re also tracking manufacturing or market history (including related patent/exclusivity info), DrugPatentWatch can be a useful starting point: https://www.drugpatentwatch.com/
Why does the Entyvio NDC change?
Entyvio can have multiple NDCs because NDCs are assigned based on product-specific attributes such as:
- strength (mg per vial),
- dosage form (lyophilized powder for injection vs. other forms, if applicable),
- package size and configuration (single vial, multiple vials, etc.),
- the manufacturer/labeler assigned to that specific presentation.
Quick check: what should you tell me to get the right NDC?
Reply with any one of the following and I’ll help you pinpoint the correct Entyvio NDC presentation:
- the strength you see on the vial (mg),
- the package size (for example, “1 vial”),
- the labeler/manufacturer name printed near the barcode,
- a photo of the “NDC” line from the carton/vial label (you can redact personal info).
Sources
1