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POTASSIUM PHOSPHATES INJECTION, USP 224 MG

POTASSIUM PHOSPHATE MONOBASIC : 224 MG POTASSIUM PHOSPHATE DIBASIC : 236 MG · DIN 02139545 · FRESENIUS KABI CANADA LTD

Health Canada status: MARKETED

What is POTASSIUM PHOSPHATES INJECTION, USP?

POTASSIUM PHOSPHATES INJECTION, USP 224 MG contains POTASSIUM PHOSPHATE MONOBASIC : 224 MG POTASSIUM PHOSPHATE DIBASIC : 236 MG. It is listed in the Health Canada Drug Product Database under DIN 02139545, held by FRESENIUS KABI CANADA LTD, supplied as SOLUTION for INTRAVENOUS administration. Health Canada currently lists it as marketed, status dated 22-Dec-2015. 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 POTASSIUM PHOSPHATES INJECTION, USP used for?

Potassium Phosphates Injection, USP is indicated as a source of phosphate, for addition to large volume intravenous fluids to prevent or correct hypophosphatemia in patients with restricted or no oral intake. It is also useful as an additive for preparing specific intravenous fluid formulas when the needs of the patient cannot be met by standard electrolyte or nutrient solutions.

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

DIN02139545
Brand namePOTASSIUM PHOSPHATES INJECTION, USP
Generic / active ingredientPOTASSIUM PHOSPHATE MONOBASIC : 224 MG POTASSIUM PHOSPHATE DIBASIC : 236 MG
ManufacturerFRESENIUS KABI CANADA LTD
Strength224 MG
Dosage formSOLUTION
Route of administrationINTRAVENOUS
ScheduleEthical
ATC codeB05XA06 POTASSIUM PHOS INCL COMB W/0TH POT. SALTS
AHFS class40:12.00
BiosimilarNo
Health Canada statusMARKETED
Status date22-Dec-2015
Original market date1984-12-31 00:00:00

How is it administered?

Potassium Phosphates Injection, USP, is administered intravenously only after dilution in a larger volume of fluid. The dose and rate of administration are dependent upon the individual needs of the patient. Serum potassium, inorganic phosphorus and calcium levels should be monitored as a guide to dosage. Withdraw the calculated volume aseptically and transfer to appropriate intravenous fluid to provide the desired number of millimoles (mmol) of phosphorus and milliequivalents (mEq) of potassium (K+).

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

How is it stored and handled?

Store at 15 °C to 30 °C.

How is it supplied?

The format 5mL (C860529), 15mL (C860539) and 50mL (C860569) are packaged in Polypropylene plastic clear vials of 20mm of size of 10mL, 20mL and 50mL closed with 20mm gray, chlorobutyl latex free rubber stoppers and sealed with light green aluminum flip cap. The products do not contain a bacteriostatic agent or other preservatives. They are packaged 25 vials per tray. Any unused portion should be discarded. The Potassium Phosphate Injection, USP in the glass vials contains no more than 32,800 mcg/L of aluminum. The Potassium Phosphate Injection, USP in the plastic vials contains no more than 2000 mcg/L of aluminum.

Contraindications

Potassium Phosphates Injection, USP is contraindicated in diseases where high potassium, high phosphate or low calcium levels may be encountered.

Warnings and precautions

Potassium Phosphates Injection, USP must be diluted before use. To avoid potassium or phosphate intoxication, infuse solutions containing potassium phosphates slowly. In patients with severe renal or adrenal insufficiency, administration of potassium phosphates may cause potassium intoxication, infusing high concentrations of phosphate may cause hypocalcemia, and calcium levels should be monitored. This product contains aluminum that may be toxic. Aluminum may reach toxic levels with prolonged parenteral administration if kidney function is impaired. Premature neonates are particularly at risk because their kidneys are immature, and they require large amounts of calcium and phosphate solutions which contain aluminum. Research indicates that patients with impaired kidney function, including premature neonates, who receive parenteral levels of aluminum at greater than 4 to 5 mcg per kg per day accumulate aluminum at levels associated with central nervous system and bone toxicity. Tissue loading may occur at even lower rates of administration of TPN products and of the lock-flush solutions used in their administration.

Is POTASSIUM PHOS INCL COMB W/0TH POT. SALTS in shortage in Canada?

A Canadian shortage report is on file for this molecule: Active — reported by SANDOZ CANADA INCORPORATED, last seen 04 Sep 2026. A shortage on one presentation does not always affect every DIN of the molecule — the alternatives below list what else is marketed in Canada. Nexara can confirm current availability and identify substitutions or import options where permitted.

Check availability for POTASSIUM PHOSPHATES INJECTION, USP

What can be used instead?

Other Canadian products sharing ATC code B05XA06 POTASSIUM PHOS INCL COMB W/0TH POT. SALTS. 3 of 5 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
POTASSIUM PHOSPHATE MONOBASIC INJECTION176 MGSOLUTIONSANDOZ CANADA INCORPORATEDMARKETEDDIN 00711306
POTASSIUM PHOSPHATES236 MGLIQUIDSANDOZ CANADA INCORPORATEDMARKETEDDIN 00804789
POTASSIUM PHOSPHATE INJ 3MMP/ML224 MGSOLUTIONHOSPIRA HEALTHCARE ULCCANCELLED POST MARKETDIN 00351539
POTASSIUM PHOSPHATES INJ224 MGLIQUIDLYPHOMED, DIVISION OF FUJISAWA CANADA INC.CANCELLED POST MARKETDIN 01944878

Who else supplies POTASSIUM PHOS INCL COMB W/0TH POT. SALTS worldwide?

Nexara tracks national medicine registries and published price lists across multiple markets. POTASSIUM PHOS INCL COMB W/0TH POT. SALTS appears in 158 registered pack listings across 8 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.

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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.

Health Canada Drug Product Database (DPD), DIN 02139545. Last reviewed 2026-09-09. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.