Prescription drug · NDA
Miebo (Perfluorohexyloctane) NDC 24208-377
Perfluorohexyloctane 1 mg/mg · Solution · Ophthalmic · Bausch & Lomb Incorporated
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 24208-377-01 | 24208037701 | 1 BOTTLE in 1 CARTON (24208-377-01) / 3 mg in 1 BOTTLEMarketed from May 18, 2023 · Sample package | |
| 24208-377-05 | 24208037705 | 1 BOTTLE in 1 CARTON (24208-377-05) / 3 mg in 1 BOTTLEMarketed from May 18, 2023 | |
| 24208-377-06 | 24208037706 | 1 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
N424208037701followed by a unit qualifier and the quantityPackage 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.
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.