JAMP HYDROXYCHLOROQUINE SULFATE 200 MG
HYDROXYCHLOROQUINE SULFATE : 200 MG · DIN 02491427 · JAMP PHARMA CORPORATION
Health Canada status: MARKETED
What is JAMP HYDROXYCHLOROQUINE SULFATE?
JAMP HYDROXYCHLOROQUINE SULFATE 200 MG contains HYDROXYCHLOROQUINE SULFATE : 200 MG. It is listed in the Health Canada Drug Product Database under DIN 02491427, held by JAMP PHARMA CORPORATION, supplied as TABLET for ORAL administration. Health Canada currently lists it as marketed, status dated 06-Feb-2020. 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 HYDROXYCHLOROQUINE SULFATE used for?
Rheumatoid arthritis, discoid and systemic lupus erythematosus in adults; treatment and suppression of acute attacks of malaria (P. vivax, P. malariae, P. ovale, susceptible P. falciparum).
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 | 02491427 |
|---|---|
| Brand name | JAMP HYDROXYCHLOROQUINE SULFATE |
| Generic / active ingredient | HYDROXYCHLOROQUINE SULFATE : 200 MG |
| Manufacturer | JAMP PHARMA CORPORATION |
| Strength | 200 MG |
| Dosage form | TABLET |
| Route of administration | ORAL |
| Schedule | Prescription |
| ATC code | P01BA02 HYDROXYCHLOROQUINE |
| AHFS class | 84:04.92 |
| Biosimilar | No |
| Health Canada status | MARKETED |
| Status date | 06-Feb-2020 |
| Original market date | 2020-01-31 00:00:00 |
How is it administered?
Adults: 200-600 mg daily depending on indication. Take with food or milk. Max daily dose 6.5 mg/kg ideal body weight. Malaria suppression: 400 mg weekly.
Included because it drives pack selection and wastage. Consult the monograph.
How is it stored and handled?
Not explicitly stated in provided text (standard section 11 was in TOC but text cut off). Standard practice is 15-30°C.
How is it supplied?
Bottles of 100 and 500 tablets.
Contraindications
Pre-existing retinopathy; hypersensitivity to 4-aminoquinolines; children under 6 years of age (weight <35 kg).
Warnings and precautions
Risk of retinopathy, cardiomyopathy, QTc prolongation, serious arrhythmias, severe hypoglycemia, bone marrow depression, and drug-induced liver injury (DILI).
What can be used instead?
Other Canadian products sharing ATC code P01BA02 HYDROXYCHLOROQUINE. 6 of 12 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 |
|---|---|---|---|---|---|
| APO-HYDROXYQUINE | 200 MG | TABLET | APOTEX INC | MARKETED | DIN 02246691 |
| HYDROXYCHLOROQUINE | 200 MG | TABLET | SANIS HEALTH INC | MARKETED | DIN 02519348 |
| MINT-HYDROXYCHLOROQUINE | 200 MG | TABLET | MINT PHARMACEUTICALS INC | MARKETED | DIN 02424991 |
| NRA-HYDROXYCHLOROQUINE | 200 MG | TABLET | NORA PHARMA INC | MARKETED | DIN 02511886 |
| PLAQUENIL | 200 MG | TABLET | SANOFI-AVENTIS CANADA INC | MARKETED | DIN 02017709 |
| ACH-HYDROXYCHLOROQUINE SULFATE | 200 MG | TABLET | ACCORD HEALTHCARE INC | APPROVED | DIN 02506696 |
| AG-HYDROXYCHLOROQUINE | 200 MG | TABLET | ANGITA PHARMA INC. | APPROVED | DIN 02510863 |
| MYLAN-HYDROXYCHLOROQUINE | 200 MG | TABLET | MYLAN PHARMACEUTICALS ULC | CANCELLED POST MARKET | DIN 02252600 |
| NU-HYDROXYQUINE | 200 MG | TABLET | NU-PHARM INC | CANCELLED (UNRETURNED ANNUAL) | DIN 02335816 |
| PMS-HYDROXYCHLOROQUINE | 200 MG | TABLET | PHARMASCIENCE INC | CANCELLED PRE MARKET | DIN 02247113 |
Who else supplies HYDROXYCHLOROQUINE worldwide?
Nexara tracks national medicine registries and published price lists across multiple markets. HYDROXYCHLOROQUINE appears in 37 registered pack listings across 9 markets, published on 6 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.