NDC codes

FDA NDC Directory
Product NDC (as listed)24208-377Labeler and product segments. Claims need a package NDC.
Product NDC at billing width24208-0377Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
24208-377-01242080377011 BOTTLE in 1 CARTON (24208-377-01) / 3 mg in 1 BOTTLEMarketed from May 18, 2023 · Sample package
24208-377-05242080377051 BOTTLE in 1 CARTON (24208-377-05) / 3 mg in 1 BOTTLEMarketed from May 18, 2023
24208-377-06242080377061 BOTTLE in 1 CARTON (24208-377-06) / 1.6 mg in 1 BOTTLEMarketed from Jul 19, 2024 · Sample package

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Miebo
Generic name (nonproprietary)
perfluorohexyloctane
Active ingredients
Perfluorohexyloctane — 1 mg/mg
Dosage form
Solution
Route
Ophthalmic
Labeler
Bausch & Lomb IncorporatedNDC labeler code 24208
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 216675
Marketing start
Listing expires
Other FDA classes
Semifluorinated Alkane (EXT)
Identifiers
Product ID 24208-377_4cb37a53-376f-ef57-e063-6294a90a5bf8SPL ID 4cb37a53-376f-ef57-e063-6294a90a5bf8SPL set ID 6b283c02-7df4-4c00-951b-555cddffe77cRxCUI 2637551, 2637556UNII 7VYX4ELWQMUPC 0324208377055
Pharmacologic class
Semifluorinated Alkane

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Ophthalmic products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N424208037701 followed by a unit qualifier and the quantity

Package 24208-0377-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

MIEBO ® (perfluorohexyloctane ophthalmic solution) is indicated for the treatment of the signs and symptoms of dry eye disease (DED). MIEBO (perfluorohexyloctane ophthalmic solution) is a semifluorinated alkane indicated for treatment of the signs and symptoms of dry eye disease. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 24208-377

What is NDC 24208-377?
24208-377 is the product NDC for Miebo (perfluorohexyloctane), Perfluorohexyloctane 1 mg/mg solution, listed with the FDA by Bausch & Lomb Incorporated. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Miebo (Perfluorohexyloctane).
What is the active ingredient?
Perfluorohexyloctane.
Who is the labeler?
Bausch & Lomb Incorporated, NDC labeler code 24208. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Miebo?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

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