See the DrugPatentWatch profile for prolia
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/