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Prescription medicine

Cenegermin Brand names: Oxervate

Cenegermin (Oxervate) is a prescription medicine. No generic is listed in FDA's NDC Directory.

  • No generic listed

Check it at the source: the cenegermin FDA label on DailyMed (effective December 31, 2024); every cenegermin label on DailyMed.

Highlights of the record

FDA label of December 31, 2024; NDC Directory, Drugs@FDA and Orange Book, October 8, 2026

Used for

From the label: indications and usage

OXERVATE ® (cenegermin-bkbj) ophthalmic solution 0.002% is indicated for the treatment of neurotrophic keratitis.

Forms and strengths

Solution/ drops; kit.

On the market

Generic approvals
No generic approved
Labelers listed (NDC)
1 of which 0 under generic applications, 1 under brand applications, repackagers included

Supply and safety

Pharmacy cost (NADAC)
Not in the survey
Shortage (FDA)
No current entry
Recalls by its makers (FDA)
No recall recorded
FAERS reports
12,024 through July 30, 2026

What is cenegermin used for?

From the label: indications and usage

OXERVATE ® (cenegermin-bkbj) ophthalmic solution 0.002% is indicated for the treatment of neurotrophic keratitis. OXERVATE is a recombinant human nerve growth factor indicated for the treatment of neurotrophic keratitis.

FDA pharmacologic class: Recombinant Human Nerve Growth Factor.

Source: FDA drug label (OXERVATE), Domp farmaceutici S.p.A., effective December 31, 2024 (SPL set 89e4bfec-d710-40ed-8885-5d13ba46b1cd), via openFDA; the full label on DailyMed

What does the patient leaflet for cenegermin say first?

The FDA-approved Medication Guide or Patient Information that comes with the medicine, in its own words.

From the patient leaflet: What should I avoid while using OXERVATE?

Your vision may be blurred for a short time after using OXERVATE. If this happens, wait until your vision clears before you drive or use machines.

Source: FDA drug label (OXERVATE), Domp farmaceutici S.p.A., effective December 31, 2024 (SPL set 89e4bfec-d710-40ed-8885-5d13ba46b1cd), via openFDA; the full label on DailyMed

Is there a generic for cenegermin (Oxervate)?

No generic cenegermin is approved (Drugs@FDA, October 8, 2026).

Source: Drugs@FDA, FDA NDC Directory and the Orange Book (openFDA bulk files, October 8, 2026)

What do FAERS reports show for cenegermin?

The FDA Adverse Event Reporting System holds 12,024 reports that list cenegermin among the medicines taken, through July 30, 2026, each a report of something that happened, not proof the medicine caused it; 211 are coded as a death and 780 as a hospital stay. Counts follow how widely a medicine is used and watched, and they are not a measure of how risky it is. Reports rose sharply in 2025 (3,179, against a median of 661 a year): FAERS counts follow reporting, which news, litigation and label changes can drive, not how often a reaction happens.

Reports received each year

The most reported reactions

  • Eye Pain (named in the label)5,863
  • Eye Irritation (named in the label)1,879
  • Product Dose Omission Issue (a use or a product term, not a reaction)1,349
  • Ocular Hyperaemia (named in the label)1,231
  • Photophobia (named in the label)1,068
  • Vision Blurred951
  • Wrong Technique In Product Usage Process (a use or a product term, not a reaction)903
  • Eye Swelling849

Side effects: the label's list and every FAERS reaction

Source: FDA Adverse Event Reporting System (FAERS) via openFDA, reports through July 30, 2026

What next?

Cenegermin side effects
the label's list beside FAERS reports
Check an interaction
what two or more labels say about each other