Prescription drug · NDA
Eysuvis (Loteprednol etabonate) NDC 71571-333
Loteprednol etabonate 2.5 mg/mL · Suspension/ drops · Ophthalmic · ALCON LABORATORIES, INC.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 71571-333-01 | 7157103330171571033301 | 1 BOTTLE, DROPPER in 1 CARTON (71571-333-01) / 1 mL in 1 BOTTLE, DROPPERMarketed from Dec 14, 2023 · Sample package | |
| 71571-333-24 | 7157103332471571033324 | 2.4 mL in 1 BOTTLE, DROPPER (71571-333-24)Marketed from Nov 18, 2020 · Sample package | |
| 71571-333-83 | 7157103338371571033383 | 1 BOTTLE, DROPPER in 1 CARTON (71571-333-83) / 8.3 mL in 1 BOTTLE, DROPPERMarketed from Nov 18, 2020 |
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)
- Eysuvis
- Generic name (nonproprietary)
- loteprednol etabonate
- Active ingredients
- Loteprednol etabonate — 2.5 mg/mL
- Dosage form
- Suspension/ drops
- Route
- Ophthalmic
- Labeler
- ALCON LABORATORIES, INC.NDC labeler code 71571
- Product type
- Prescription drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 210933
- Marketing start
- Listing expires
- Other FDA classes
- Corticosteroid Hormone Receptor Agonists (Mechanism)
- Identifiers
- Product ID 71571-333_db147c65-ed03-4af5-af1f-86b9ff51148aSPL ID db147c65-ed03-4af5-af1f-86b9ff51148aSPL set ID a2169d82-4275-4ab6-a1c3-c274080b815cRxCUI 2464838, 2464843UNII YEH1EZ96K6
- Pharmacologic class
- Corticosteroid
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
N471571033301followed by a unit qualifier and the quantityPackage 71571-0333-01. 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)
EYSUVIS is a corticosteroid indicated for the short-term (up to two weeks) treatment of the signs and symptoms of dry eye disease. EYSUVIS is a corticosteroid indicated for the short-term (up to two weeks) treatment of the signs and symptoms of dry eye disease. ( 1 )
Excerpt only. Read the full label for complete information.
About NDC 71571-333
- What is NDC 71571-333?
- 71571-333 is the product NDC for Eysuvis (loteprednol etabonate), Loteprednol etabonate 2.5 mg/mL suspension/ drops, listed with the FDA by ALCON LABORATORIES, INC.. It has 3 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Eysuvis (Loteprednol etabonate).
- What is the active ingredient?
- Loteprednol etabonate.
- Who is the labeler?
- ALCON LABORATORIES, INC., NDC labeler code 71571. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Eysuvis?
- 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.