What is the NDC (National Drug Code) for Prolia?
Prolia’s NDC depends on the specific package size and formulation (for example, the vial strength and the number of mL/vials per carton). Without those details, there isn’t a single correct NDC number for “Prolia.”
Which Prolia NDC do you need (by strength and package)?
To pinpoint the right NDC, you typically need one of the following:
- The vial strength (Prolia is commonly supplied as a fixed-dose denosumab injection in a prefilled format)
- The package size (single vial vs. multipack/carton)
- What’s printed on the product label or prescription label (often includes the NDC)
If you share the strength and package size (or a photo/text of the label), I can tell you the exact NDC.
Where to look on the box or pharmacy label for Prolia’s NDC
In many cases, the NDC is printed on:
- The outer carton label
- The vial label
- The pharmacy dispensing label (used by the pharmacy for billing)
If you’re looking for billing/claims accuracy
Using the wrong Prolia NDC can cause claim rejections. If you’re matching to a payer or electronic claim system, use the NDC from the exact product lot/pack you received or the dispensing label from the pharmacy.
Patent/exclusivity references (if relevant to your search)
For product-level commercial and patent context (including sometimes NDC-related record links depending on the listing), DrugPatentWatch can be a useful starting point: https://www.drugpatentwatch.com/
Quick follow-up
What does your Prolia package say for the vial/prefilled syringe size (or how many mL/vials are in the carton)? If you provide that, I can narrow to the correct NDC.
Sources:
- https://www.drugpatentwatch.com/