Skip to content
MedsAcross

Medicine

Qlosi 4 mg/mL ophthalmic solution

Pilocarpine · Ophthalmic · Orasis Pharmaceuticals
Available on requestPrescription onlyUS FDA Cold chain

Qlosi 4 mg/mL ophthalmic solution is a prescription medicine containing Pilocarpine for ophthalmic use, marketed by Orasis Pharmaceuticals, 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 refrigerated at 36°F to 46°F (2°C to 8°C). Once a pouch is open, the…

Key facts

Active ingredient (INN)
Pilocarpine
Brand
Qlosi
Strength
4 mg/mL
Dosage form
Ophthalmic solution
Route
Ophthalmic
Packs
10 vials, 20 vials, 30 vials and 1 more
Marketing authorisation holder
Orasis Pharmaceuticals
Manufacturer
Orasis Pharmaceuticals
Origin register
US FDA, United States
Storage
Store refrigerated at 36°F to 46°F (2°C to 8°C). Once a pouch is open, the single-patient-use vials may be stored at room temperature [up to 77°F (25°C)] and used within 30 days. Store unused product away from light.
Cold chain
Yes, shipped temperature controlled
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
N07AX01 Pilocarpine
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
15 October 2024
Identifiers
RxCUI 2695439, 2695445DailyMed set ID 4ee2a840-1203-473a-aa42-316a3ddf2fbeNDC 83661-018Application NDA217836

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
10 vial, single-use in 1 box / .4 mL in 1 vial, single-use83661-018-10Orasis Pharmaceuticals15 January 2025
20 vial, single-use in 1 box / .4 mL in 1 vial, single-use83661-018-20Orasis Pharmaceuticals15 January 2025
30 vial, single-use in 1 box / .4 mL in 1 vial, single-use83661-018-30Orasis Pharmaceuticals15 October 2024
60 vial, single-use in 1 box / .4 mL in 1 vial, single-use83661-018-60Orasis Pharmaceuticals15 January 2025

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 29 July 1974Drugs@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

Other strengths and forms of Pilocarpine

Clinical summary

Pilocarpine is a cholinergic receptor agonist. It is available as tablets, eye drops and ophthalmic solution for oral use. MedsAcross supplies Pilocarpine 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 Pilocarpine

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

Data sources

Need Qlosi 4 mg/mL ophthalmic 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.