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Molecule

Nerandomilast

Presentations
2
Brands
1
Manufacturers
1
Available from stock
0

Nerandomilast is a prescription medicine indicated for the treatment of idiopathic pulmonary fibrosis in adult patients, among other approved uses. It is available as tablets for oral use. MedsAcross supplies Nerandomilast for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Key facts

ATC classification
L04AA61 Nerandomilast · Immunosuppressive drug, subgroup L04AA
US FDA first approval
7 October 2025
EU status
Authorised
Orphan designation
Yes
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Oral
Dosage forms
Tablet
Identifiers
UNII I5DGT51IB8

Clinical information

From the regulator-approved product information. Each section names its source.

Uses

JASCAYD is a phosphodiesterase 4 (PDE4) inhibitor indicated for: The treatment of idiopathic pulmonary fibrosis in adult patients. The treatment of progressive pulmonary fibrosis in adult patients.

Source: US FDA prescribing information

How it works

Nerandomilast is an inhibitor of phosphodiesterase 4 (PDE4) with at least nine-fold preferential inhibition of the PDE4B isoenzyme over PDE4A, PDE4C, and PDE4D based on in vitro data. PDE4 hydrolyzes and inactivates cyclic adenosine monophosphate (cAMP). Nerandomilast exerts both antifibrotic and immunomodulatory effects as PDE4B inhibition elevates intracellular cAMP levels and reduces the expression of profibrotic growth factors and inflammatory cytokines, which are overexpressed in IPF and PPF.

Source: US FDA prescribing information

Dosing overview

Recommended Dosage: 18 mg orally twice daily approximately 12 hours apart with or without food. Reduce JASCAYD to 9 mg twice daily for patients who are unable to tolerate 18 mg twice daily, except in patients taking concomitant moderate CYP3A inducers or pirfenidone. Swallow tablets whole or dispersed in water. See full prescribing information for dosage modification for concomitant use with CYP3A inhibitors and administration instructions for patients who have difficulty swallowing tablets.

Source: US FDA prescribing information

Side effects

Most common adverse reactions (≥5%) are diarrhea, COVID-19, upper respiratory tract infection, depression, weight decreased, decreased appetite, nausea, fatigue, headache, vomiting, back pain, and dizziness.

Source: US FDA prescribing information

Interactions

Strong CYP3A Inhibitors: Reduce JASCAYD dosage to 9 mg twice daily. Strong CYP3A Inducers: Avoid concomitant use with JASCAYD. Moderate CYP3A Inducers: Recommended dosage is 18 mg twice daily. Do not reduce dosage to 9 mg twice daily.

Source: US FDA prescribing information

Storage

Store at 20°C to 25°C (68°F to 77°F), excursions permitted to 15°C to 30°C (59°F to 86°F). Store in the original container to protect from light.

Source: US FDA prescribing information

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

All presentations

2 presentations of Nerandomilast, sorted by availability.

MedicineManufacturerRegisterAvailability
Jascayd 18 mg tabletOralBoehringer Ingelheim PharmaceuticalsUS FDAAvailable on request
Jascayd 9 mg tabletOralBoehringer Ingelheim PharmaceuticalsUS FDAAvailable on request

Brands by market

1 brand names across 1 markets.

Brand names by country

United States

Manufacturers

Regulatory status

Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.

RegisterStatusSource
US FDAFirst approved 7 October 2025Drugs@FDA
EU (EMA)AuthorisedEMA medicines data
India (CDSCO)Not yet confirmed against CDSCO approval lists—
AustriaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BelgiumRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
BulgariaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CroatiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CyprusRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
CzechiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
DenmarkRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
EstoniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FinlandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
FranceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GermanyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
GreeceRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
HungaryRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IcelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
IrelandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
ItalyRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LatviaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LiechtensteinRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LithuaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
LuxembourgRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
MaltaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NetherlandsRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
NorwayRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PolandRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
PortugalRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
RomaniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SlovakiaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SloveniaRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SpainRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
SwedenRegisteredEuropean Medicines Agency (central authorisation)Checked 12 November 2026
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Questions and answers

Is Nerandomilast available for export from India?

Yes, on request. MedsAcross lists 2 presentations of Nerandomilast and sources them for licensed hospitals, importers and physicians against valid import documents.

What brand names does Nerandomilast have?

The catalogue lists 1 brand names for Nerandomilast, including Jascayd.

Is Nerandomilast approved by the US FDA?

Yes. The US FDA first approved Nerandomilast on 7 October 2025, according to Drugs@FDA.

Is Nerandomilast authorised in the European Union?

Yes. Nerandomilast has a central EU marketing authorisation (status: authorised), according to European Medicines Agency data.

Does Nerandomilast need cold chain shipping?

No listed presentation of Nerandomilast is recorded as needing a cold chain. Storage conditions are shown on each presentation page.

Which ATC class is Nerandomilast in?

Nerandomilast is classified under ATC code L04AA61 (Nerandomilast).

References

  1. JASCAYD prescribing information (Boehringer Ingelheim Pharmaceuticals). U.S. National Library of Medicine, DailyMed. Retrieved 14 August 2026
  2. Jascayd: European public assessment report (EPAR). European Medicines Agency. Retrieved 9 November 2026

Request Nerandomilast for export supply

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