JAMPLYTE 0.76 G
POTASSIUM CHLORIDE : 0.76 G SODIUM BICARBONATE : 1.69 G SODIUM CHLORIDE : 1.46 G SODIUM SULFATE : 5.74 G POLYETHYLENE GLYCOL 3350 : 59.55 G · DIN 02368234 · JAMP PHARMA CORPORATION
Health Canada status: APPROVED
What is JAMPLYTE?
JAMPLYTE 0.76 G contains POTASSIUM CHLORIDE : 0.76 G SODIUM BICARBONATE : 1.69 G SODIUM CHLORIDE : 1.46 G SODIUM SULFATE : 5.74 G POLYETHYLENE GLYCOL 3350 : 59.55 G. It is listed in the Health Canada Drug Product Database under DIN 02368234, held by JAMP PHARMA CORPORATION, supplied as POWDER FOR SOLUTION for ORAL administration. Health Canada currently lists it as approved, status dated 12-May-2011. 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.
Product details and regulatory record
| DIN | 02368234 |
|---|---|
| Brand name | JAMPLYTE |
| Generic / active ingredient | POTASSIUM CHLORIDE : 0.76 G SODIUM BICARBONATE : 1.69 G SODIUM CHLORIDE : 1.46 G SODIUM SULFATE : 5.74 G POLYETHYLENE GLYCOL 3350 : 59.55 G |
| Manufacturer | JAMP PHARMA CORPORATION |
| Strength | 0.76 G |
| Dosage form | POWDER FOR SOLUTION |
| Route of administration | ORAL |
| Schedule | Ethical |
| ATC code | A06AD65 MACROGOL, COMBINATIONS |
| AHFS class | 56:12.00 |
| Biosimilar | No |
| Health Canada status | APPROVED |
| Status date | 12-May-2011 |
What can be used instead?
Other Canadian products sharing ATC code A06AD65 MACROGOL, COMBINATIONS. 3 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.
| Product | Strength | Form | Manufacturer | Health Canada status | DIN |
|---|---|---|---|---|---|
| COLYTE | 10.65 MG | POWDER FOR SOLUTION | PENDOPHARM DIVISION OF PHARMASCIENCE INC | MARKETED | DIN 00677442 |
| JAMPLYTE | 22.96 G / 280 G | POWDER | JAMP PHARMA CORPORATION | MARKETED | DIN 02378329 |
| MOVIPREP | 2.691 G | POWDER FOR SOLUTION | ARALEZ PHARMACEUTICALS CANADA INC | MARKETED | DIN 02359499 |
| JAMP-ELECTROPEG | 2.97 G | POWDER FOR SOLUTION | JAMP PHARMA CORPORATION | APPROVED | DIN 02406780 |
| JAMP-ELECTROPEG WITH FLAVOUR PACKET | 2.97 G | POWDER FOR SOLUTION | JAMP PHARMA CORPORATION | APPROVED | DIN 02406799 |
| KLEAN-PREP | 1.68 G | POWDER FOR SOLUTION | PENDOPHARM DIVISION OF PHARMASCIENCE INC | CANCELLED POST MARKET | DIN 02147793 |
| PLENVU | 9 G | KIT ; POWDER FOR SOLUTION | BAUSCH HEALTH, CANADA INC. | CANCELLED PRE MARKET | DIN 02550938 |
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.