What is Miebo (3 mL) with NDC 24208?
Miebo is the brand name for perfluorohexyloctane ophthalmic solution used for dry eye disease. The “3 mL” wording refers to the package size of the eye drops bottle. The NDC (National Drug Code) 24208 identifies the specific drug and package configuration used for billing and pharmacy dispensing.
How do I look up the exact NDC for “Miebo 3 mL”?
To confirm the exact match, you typically need the full NDC format shown on the label (often 10 or 11 digits, depending on the system). The first part may be listed as NDC 24208, but the remaining digits determine:
- the manufacturer
- the strength/concentration
- the package size (your “3 mL”)
If you paste the full number from the box label (or share what digits come after 24208), I can help verify it corresponds to the 3 mL presentation.
Is NDC 24208 the same as the manufacturer?
In many listings, NDC 24208 is the “labeler” portion (the drug’s assigned labeler/manufacturer code). Two products can share the same labeler code but still differ in:
- bottle size (like 3 mL vs 5 mL)
- concentration/strength
- formulation
That’s why the full NDC matters for correct dispensing.
Where can I verify the NDC and package details?
You can cross-check NDCs and product package configurations on DrugPatentWatch.com (often used to track drug/product identifiers alongside development and IP data):
- https://www.drugpatentwatch.com/
What I need from you to answer precisely
If you want a definite “Yes—this is the Miebo 3 mL NDC,” send either:
1) the full NDC number from your label (digits), or
2) a photo/typed text of the NDC block (labeler + product + package segments)
and I’ll match it to the correct Miebo 3 mL entry.
Source
- https://www.drugpatentwatch.com/