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UPTRAVI 400 MCG

SELEXIPAG : 400 MCG · DIN 02451166 · JANSSEN INC

Health Canada status: MARKETED

What is UPTRAVI?

UPTRAVI 400 MCG contains SELEXIPAG : 400 MCG. It is listed in the Health Canada Drug Product Database under DIN 02451166, held by JANSSEN INC, supplied as TABLET for ORAL administration. Health Canada currently lists it as marketed, status dated 16-Dec-2019. Nexara Health is a licensed Canadian wholesale distributor (DEL 3-002896-A) and can source this product for hospitals, pharmacies and clinics. Availability and lead time are confirmed per order.

What is UPTRAVI used for?

Long-term treatment of PAH (idiopathic, heritable, associated with connective tissue disorders or congenital heart disease) in adults with WHO FC II–III to delay disease progression.

Authorized indication as written in the Health Canada product monograph. For healthcare professionals and licensed purchasers; this is not medical advice.

Product details and regulatory record

DIN02451166
Brand nameUPTRAVI
Generic / active ingredientSELEXIPAG : 400 MCG
ManufacturerJANSSEN INC
Strength400 MCG
Dosage formTABLET
Route of administrationORAL
SchedulePrescription
ATC codeB01AC27 SELEXIPAG
AHFS class48:48.00
BiosimilarNo
Health Canada statusMARKETED
Status date16-Dec-2019
Original market date2016-04-21 00:00:00

How is it administered?

Starting dose 200 mcg twice daily. Titrate by 200 mcg increments weekly to highest tolerated dose, max 1600 mcg twice daily. Reduce frequency to once daily in moderate hepatic impairment.

Included because it drives pack selection and wastage. Consult the monograph.

How is it stored and handled?

Not explicitly detailed in provided text (section 11 header present but content truncated), though packaging includes desiccant.

How is it supplied?

Alu/Alu blister with desiccant in cartons of 60 film-coated tablets.

Contraindications

Hypersensitivity to selexipag or any ingredient; Concomitant use of strong inhibitors of CYP2C8 (e.g., gemfibrozil).

Warnings and precautions

Vasodilatory effects (hypotension); pulmonary oedema (consider PVOD); hyperthyroidism (monitor thyroid function); increased exposure in moderate hepatic impairment.

What can be used instead?

Other Canadian products sharing ATC code B01AC27 SELEXIPAG. 8 of 8 DINs in this group are currently marketed — marketed products are listed first, because that is what can actually be bought. These tables describe supply, not clinical equivalence: substitution rests with the prescriber or pharmacist, and interchangeability is determined provincially.

ProductStrengthFormManufacturerHealth Canada statusDIN
UPTRAVI1000 MCGTABLETJANSSEN INCMARKETEDDIN 02451190
UPTRAVI1200 MCGTABLETJANSSEN INCMARKETEDDIN 02451204
UPTRAVI1400 MCGTABLETJANSSEN INCMARKETEDDIN 02451212
UPTRAVI1600 MCGTABLETJANSSEN INCMARKETEDDIN 02451220
UPTRAVI200 MCGTABLETJANSSEN INCMARKETEDDIN 02451158
UPTRAVI600 MCGTABLETJANSSEN INCMARKETEDDIN 02451174
UPTRAVI800 MCGTABLETJANSSEN INCMARKETEDDIN 02451182

Who else supplies SELEXIPAG worldwide?

Nexara tracks national medicine registries and published price lists across multiple markets. SELEXIPAG appears in 113 registered pack listings across 12 markets, published on 9 different national price bases. Where a Canadian route is closed, that is where an alternative route of supply starts — subject to the import rules in both countries.

Registered listings are not stock. Ask us to confirm what can actually be sourced for your order.

How can I get it?

Nexara Health supplies this product to licensed Canadian buyers — pharmacies, hospitals, clinics, licensed distributors, and clinical trial sponsors or their CROs. We confirm stock, pack size, expiry and pricing at the time of quotation. If the product is on backorder or in shortage, we identify equivalent alternatives and import options where permitted.

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Ordering questions

Who can buy this from Nexara?

Licensed entities only. Nexara holds Health Canada establishment licence DEL 3-002896-A and ships only to a licensed address.

Is there a minimum order?

Yes, set per product line and per pack multiple rather than on the order total, so you are never asked to buy a part-pack. The minimum for this line is confirmed with your quote.

What is the lead time?

Confirmed per order at quotation, and it depends on current stock position and whether the product is in shortage.

Can Nexara supply this for a clinical trial?

Yes — comparator and background-therapy supply, including sourcing from other markets where a Canadian pack will not satisfy the protocol. Clinical trial supply.

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Health Canada Drug Product Database (DPD), DIN 02451166. Last reviewed 2026-09-08. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.