JAMP-QUININE 300 MG
QUININE SULFATE : 300 MG · DIN 02445204 · JAMP PHARMA CORPORATION
Health Canada status: DORMANT
What is JAMP-QUININE?
JAMP-QUININE 300 MG contains QUININE SULFATE : 300 MG. It is listed in the Health Canada Drug Product Database under DIN 02445204, held by JAMP PHARMA CORPORATION, supplied as CAPSULE for ORAL administration. Health Canada currently lists it as dormant, status dated 03-Sep-2025. 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 JAMP-QUININE used for?
In combination with a second antimalarial drug for the treatment of uncomplicated Plasmodium falciparum malaria. Not for prevention or treatment of nocturnal leg cramps.
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
| DIN | 02445204 |
|---|---|
| Brand name | JAMP-QUININE |
| Generic / active ingredient | QUININE SULFATE : 300 MG |
| Manufacturer | JAMP PHARMA CORPORATION |
| Strength | 300 MG |
| Dosage form | CAPSULE |
| Route of administration | ORAL |
| Schedule | Prescription |
| ATC code | P01BC01 QUININE |
| AHFS class | 08:30.08 |
| Biosimilar | No |
| Health Canada status | DORMANT |
| Status date | 03-Sep-2025 |
| Original market date | 2015-09-16 00:00:00 |
How is it administered?
Adults: 600 mg every 8 hours for 3-7 days. Children: 9 mg/kg (max 600 mg) every 8 hours for 3-7 days. Take with food. Dosage adjustment required for severe renal impairment.
Included because it drives pack selection and wastage. Consult the monograph.
How is it stored and handled?
Store at room temperature, 15-30ºC, in a dry place.
How is it supplied?
Bottles of 100 and 500 capsules.
Contraindications
Hypersensitivity to quinine/ingredients; QT prolongation; G6PD deficiency; myasthenia gravis; optic neuritis; history of quinine-induced thrombocytopenia or blackwater fever.
Warnings and precautions
Serious hematologic reactions (thrombocytopenia, HUS/TTP) if used for leg cramps. Risk of QT prolongation and ventricular arrhythmias. May exacerbate myasthenia gravis.
What can be used instead?
Other Canadian products sharing ATC code P01BC01 QUININE. 4 of 19 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.
| Product | Strength | Form | Manufacturer | Health Canada status | DIN |
|---|---|---|---|---|---|
| PRO-QUININE - 200 | 200 MG | CAPSULE | PRO DOC LIMITEE | MARKETED | DIN 02311216 |
| PRO-QUININE - 300 | 300 MG | CAPSULE | PRO DOC LIMITEE | MARKETED | DIN 02311224 |
| TEVA-QUININE | 200 MG | CAPSULE | TEVA CANADA LIMITED | MARKETED | DIN 00021008 |
| TEVA-QUININE | 300 MG | CAPSULE | TEVA CANADA LIMITED | MARKETED | DIN 00021016 |
| APO-QUININE | 200 MG | CAPSULE | APOTEX INC | DORMANT | DIN 02254514 |
| APO-QUININE | 300 MG | CAPSULE | APOTEX INC | DORMANT | DIN 02254522 |
| JAMP-QUININE | 200 MG | CAPSULE | JAMP PHARMA CORPORATION | DORMANT | DIN 02445190 |
| QUININE - ODAN | 200 MG | CAPSULE | ODAN LABORATORIES LTD | DORMANT | DIN 00695440 |
| QUININE - ODAN | 300 MG | TABLET | ODAN LABORATORIES LTD | DORMANT | DIN 00695432 |
| QUININE - ODAN | 300 MG | CAPSULE | ODAN LABORATORIES LTD | DORMANT | DIN 00695459 |
Who else supplies QUININE worldwide?
Nexara tracks national medicine registries and published price lists across multiple markets. QUININE appears in 4 registered pack listings across 2 markets, published on 2 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.
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.