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Molecule

Dornase alfa

Recombinant Human Deoxyribonuclease 1
Available on requestBiologicOrphanCold chain
Presentations
1
Brands
1
Manufacturers
1
Available from stock
0

Dornase alfa is a recombinant human deoxyribonuclease 1 indicated , in conjunction with standard therapies, for the management of pediatric and adult patients with cystic fibrosis (CF) to improve pulmonary function. MedsAcross supplies Dornase alfa 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

Pharmacological class
Recombinant Human Deoxyribonuclease 1, Decreased Respiratory Secretion Viscosity
US FDA first approval
30 December 1993
EU status
Not recorded
Orphan designation
Yes
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Inhalation
Dosage forms
Inhalation solution
Biologic
Yes
Identifiers
UNII 953A26OA1YRxCUI 337623CAS 9003-98-9DrugBank DB00003Q2067922

Clinical information

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

Uses

PULMOZYME ® is indicated, in conjunction with standard therapies, for the management of pediatric and adult patients with cystic fibrosis (CF) to improve pulmonary function. In CF patients with an FVC ≥ 40% of predicted, daily administration of PULMOZYME has also been shown to reduce the risk of respiratory tract infections requiring parenteral antibiotics. PULMOZYME is a recombinant DNase enzyme indicated in conjunction with standard therapies for the management of cystic fibrosis (CF) patients to improve pulmonary function.

Source: US FDA prescribing information

How it works

PULMOZYME is recombinant human deoxyribonuclease I (rhDNase), an enzyme which selectively cleaves DNA. In preclinical in vitro studies, PULMOZYME hydrolyzes the DNA in sputum of CF patients and reduces sputum viscoelasticity. In CF patients, retention of viscous purulent secretions in the airways contributes both to reduced pulmonary function and to exacerbations of infection. Purulent pulmonary secretions contain very high concentrations of extracellular DNA released by degenerating leukocytes that accumulate in response to infection.

Source: US FDA prescribing information

Dosing overview

The recommended dosage is 2.5 mg (one single-dose ampule) inhaled once daily using a recommended nebulizer. Some patients may benefit from twice daily administration. See full prescribing information for the recommended nebulizers for use with PULMOZYME.

Source: US FDA prescribing information

Contraindications

PULMOZYME is contraindicated in patients with known hypersensitivity to dornase alfa, Chinese Hamster Ovary cell products, or any component of the product.

Source: US FDA prescribing information

Side effects

The most common adverse reactions (occurring in ≥3% of patients treated with PULMOZYME over placebo) seen in clinical trials in CF patients were: voice alteration, pharyngitis, rash, laryngitis, chest pain, conjunctivitis, rhinitis, decrease in FVC of ≥10%, fever, and dyspnea.

Source: US FDA prescribing information

Storage

Store PULMOZYME ampules at a refrigerated temperature between 2°C to 8°C (36°F to 46°F) in their protective foil to protect from light and heat. Once the protective foil pouch is opened, the unused ampules must be kept refrigerated in the protective foil pouch to protect from light and heat. During transport, keep the ampules refrigerated in their protective foil pouch to protect from light and heat. Do not use if the ampules are exposed to room temperature (22°C to 28°C [72°F to 82°F]) for more than a total of 60 hours.

Source: US FDA prescribing information

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

All presentations

1 presentations of Dornase alfa, sorted by availability.

MedicineManufacturerRegisterAvailability
Pulmozyme 1 mg/mL inhalation solutionInhalation Cold chainGenentechUS 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 30 December 1993Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Conditions

Conditions linked to Dornase alfa in public data. This is not a list of approved uses, see the clinical information.

Questions and answers

Is Dornase alfa available for export from India?

Yes, on request. MedsAcross lists 1 presentations of Dornase alfa and sources them for licensed hospitals, importers and physicians against valid import documents.

What brand names does Dornase alfa have?

The catalogue lists 1 brand names for Dornase alfa, including Pulmozyme.

Is Dornase alfa approved by the US FDA?

Yes. The US FDA first approved Dornase alfa on 30 December 1993, according to Drugs@FDA.

Does Dornase alfa need cold chain shipping?

At least one listed presentation of Dornase alfa must be kept cold, so it is shipped in temperature-controlled packaging. Check the storage line on each presentation.

References

  1. Pulmozyme prescribing information (Genentech). U.S. National Library of Medicine, DailyMed. Retrieved 17 December 2025

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