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TORADOL 10 MG

KETOROLAC TROMETHAMINE : 10 MG · DIN 02162660 · AA PHARMA INC

Health Canada status: MARKETED

What is TORADOL?

TORADOL 10 MG contains KETOROLAC TROMETHAMINE : 10 MG. It is listed in the Health Canada Drug Product Database under DIN 02162660, held by AA PHARMA INC, supplied as TABLET for ORAL administration. Health Canada currently lists it as marketed, status dated 30-Jul-2018. 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 TORADOL used for?

Short-term management of moderate to moderately severe acute pain, including post-surgical, acute musculoskeletal trauma, and post-partum uterine cramping pain. Not to exceed 5-7 days.

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

DIN02162660
Brand nameTORADOL
Generic / active ingredientKETOROLAC TROMETHAMINE : 10 MG
ManufacturerAA PHARMA INC
Strength10 MG
Dosage formTABLET
Route of administrationORAL
SchedulePrescription
ATC codeM01AB15 KETOROLAC
AHFS class28:08.04.92
BiosimilarNo
Health Canada statusMARKETED
Status date30-Jul-2018
Original market date1995-12-31 00:00:00

How is it administered?

Usual dose: 10 mg every 4-6 hours as required. Max 40 mg/day. Max duration: 5 days for post-surgical pain, 7 days for musculoskeletal pain. Take with meals.

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 mentioned but content not visible), though standard House Standard applies.

How is it supplied?

Bottles of 100 tablets.

Contraindications

Hypersensitivity to ketorolac or NSAIDs; CABG surgery; 3rd trimester pregnancy; labour/delivery; breastfeeding; severe HF; active peptic ulcer/GI bleed; inflammatory bowel disease; coagulation disorders.

Warnings and precautions

Serious CV risk (MI, stroke); Serious GI risk (bleeding, ulceration, perforation); Risk of fluid retention and edema; Renal effects; Inhibits platelet function.

Is KETOROLAC in shortage in Canada?

A Canadian shortage report is on file for this molecule: Active — reported by AA PHARMA INC (Tier 3 Drug Shortages About & Resources), 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.

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What can be used instead?

Other Canadian products sharing ATC code M01AB15 KETOROLAC. 8 of 25 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
APO-KETOROLAC10 MGTABLETAPOTEX INCMARKETEDDIN 02229080
JAMP KETOROLAC10 MGTABLETJAMP PHARMA CORPORATIONMARKETEDDIN 02510855
KETOROLAC TROMETHAMINE INJECTION, USP30 MGSOLUTIONJUNO PHARMACEUTICALS CORP.MARKETEDDIN 02443376
KETOROLAC TROMETHAMINE INJECTION, USP30 MGLIQUIDFRESENIUS KABI CANADA LTDMARKETEDDIN 02244947
MAR-KETOROLAC10 MGTABLETMARCAN PHARMACEUTICALS INCMARKETEDDIN 02465124
MINT-KETOROLAC10 MGTABLETMINT PHARMACEUTICALS INCMARKETEDDIN 02461455
TORADOL IM10 MGSOLUTIONATNAHS PHARMA UK LIMITEDMARKETEDDIN 02162644
APO-KETOROLAC INJECTABLE30 MGSOLUTIONAPOTEX INCDORMANTDIN 02243989
KETOROLAC TROMETHAMINE INJECTION USP10 MGLIQUIDSABEX INCCANCELLED PRE MARKETDIN 02239943
KETOROLAC TROMETHAMINE INJECTION USP30 MGSOLUTIONSTERIMAX INCAPPROVEDDIN 02461129

Who else supplies KETOROLAC worldwide?

Nexara tracks national medicine registries and published price lists across multiple markets. KETOROLAC appears in 48 registered pack listings across 10 markets, published on 8 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 02162660. Last reviewed 2026-09-08. Nexara Health is a licensed wholesaler and supplies licensed entities only; consumer orders are routed to a partner pharmacy.