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Medicine

Perforomist 20 mcg/2 mL inhalation solution

Formoterol · Inhalation · Viatris Specialty
Available on requestPrescription onlyUS FDA Cold chain

Perforomist 20 mcg/2 mL inhalation solution is a prescription medicine containing Formoterol for inhalation use, marketed by Viatris Specialty, with its source record on the US FDA register. It is available on request for export supply from India to licensed hospitals, importers and physicians. It ships in a temperature-controlled cold chain.

Availability

Available on request

Export supply from India to licensed buyers

Typical lead time

On request

Counted from payment and complete documents

Shipping

Cold chain

Store in a refrigerator, 2°C to 8°C (36°F to 46°F). After dispensing to the…

Key facts

Active ingredient (INN)
Formoterol
Brand
Perforomist
Strength
20 mcg/2 mL
Dosage form
Inhalation solution
Route
Inhalation
Packs
30 pouches, 60 pouches
Marketing authorisation holder
Viatris Specialty
Manufacturer
Viatris Specialty
Origin register
US FDA, United States
Storage
Store in a refrigerator, 2°C to 8°C (36°F to 46°F). After dispensing to the patient: Store in a refrigerator at 2°C to 8°C (36°F to 46°F) and discard when drug expires or store at room temperature, 20°C to 25°C (68°F to 77°F) and discard if not used after 3 months.
Cold chain
Yes, shipped temperature controlled
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
R03AC13 Formoterol
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
1 October 2007
Identifiers
RxCUI 1246319, 1246321DailyMed set ID fb2fe258-fe2e-47f6-8adf-ca75bf6f90afNDC 49502-605Application NDA022007

Record updated 12 November 2026

Documents available

Documents that can be provided with this medicine. Your regulator may ask for more, and the quote lists the full set.

No document list is recorded for this medicine yet. Tell us which documents your regulator needs (for example a CoA, COPP or GMP certificate) when you request a quote.

Packs

PackCodeLabelerMarketed since
30 pouch in 1 carton / 1 vial in 1 pouch / 2 mL in 1 vial49502-605-30Viatris Specialty1 October 2007
60 pouch in 1 carton / 1 vial in 1 pouch / 2 mL in 1 vial49502-605-61Viatris Specialty1 October 2007

Status by register

Where this medicine is registered, from the source record and the regulator data we hold. Ask us about a country that is not listed.

RegisterStatusSource
US FDAListed, marketedSource record for this pageChecked 12 November 2026
US FDAFirst approved 16 February 2001Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Import route

Pick the destination country to see the legal import route, who applies and typical timelines, from our import guide for that country.

Import guides are available for 25 countries. Pick one to see its route summary.

BrazilColombiaEgyptEthiopiaGhanaIraqKazakhstanKenyaAll import guides

Alternatives

Other makers and brands of Formoterol 20 mcg/2 mL inhalation solution.

Compare 1

Clinical summary

Formoterol is a beta2-adrenergic agonist indicated for long-term, twice daily (morning and evening) administration in the maintenance treatment of bronchoconstriction in patients with chronic obstructive pulmonary disease (COPD), including chronic bronchitis and emphysema, among other approved uses. MedsAcross supplies Formoterol 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

Read about Formoterol

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

Data sources

Need Perforomist 20 mcg/2 mL inhalation solution for your hospital or patient?

Send one request with the destination country and quantity. We confirm availability, lead time and the documents your regulator needs.