KETOPROFEN SR 200 MG
KETOPROFEN : 200 MG · DIN 02172577 · AA PHARMA INC
Health Canada status: MARKETED
What is KETOPROFEN SR?
KETOPROFEN SR 200 MG contains KETOPROFEN : 200 MG. It is listed in the Health Canada Drug Product Database under DIN 02172577, held by AA PHARMA INC, supplied as TABLET (EXTENDED-RELEASE) for ORAL administration. Health Canada currently lists it as marketed, status dated 01-Jun-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.
What is KETOPROFEN SR used for?
KETOPROFEN, KETOPROFEN-E and KETOPROFEN SR are indicated for the treatment of the signs and symptoms of rheumatoid arthritis, osteoarthritis, the treatment of primary dysmenorrhea, and the relief of mild to moderate acute pain associated with musculotendinous trauma (sprains and strains), postoperative (including dental surgery) or postpartum pain. As NSAIDs, they only relieve symptoms and decrease inflammation for as long as the patient continues to take it; they do not treat clinical disease or prevent its progression.
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 | 02172577 |
|---|---|
| Brand name | KETOPROFEN SR |
| Generic / active ingredient | KETOPROFEN : 200 MG |
| Manufacturer | AA PHARMA INC |
| Strength | 200 MG |
| Dosage form | TABLET (EXTENDED-RELEASE) |
| Route of administration | ORAL |
| Schedule | Prescription |
| ATC code | M01AE03 KETOPROFEN |
| Biosimilar | No |
| Health Canada status | MARKETED |
| Status date | 01-Jun-2011 |
How is it stored and handled?
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How is it supplied?
KETOPROFEN 50 mg capsules: bottles of 100, 500 and 1000. KETOPROFEN-E 50 mg enteric-coated tablets: bottles of 100, 500 and 1000. KETOPROFEN-E 100 mg tablets: bottles of 100, 500 and 1000. KETOPROFEN SR 200 mg tablets: bottles of 100 and 500, and unit dose packages of 100 (10x10).
What can be used instead?
Other Canadian products sharing ATC code M01AE03 KETOPROFEN. 3 of 36 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 |
|---|---|---|---|---|---|
| KETOPROFEN-E | 100 MG | TABLET (ENTERIC-COATED) | AA PHARMA INC | MARKETED | DIN 00842664 |
| KETOPROFEN-E | 50 MG | TABLET (ENTERIC-COATED) | AA PHARMA INC | MARKETED | DIN 00790435 |
| KETOPROFEN | 50 MG | CAPSULE | AA PHARMA INC | DORMANT | DIN 00790427 |
| KETOPROFEN SUPPOSITORIES | 100 MG | SUPPOSITORY | PHARMEL INC | CANCELLED POST MARKET | DIN 02237011 |
| KETOPROFEN SUPPOSITORIES | 50 MG | SUPPOSITORY | PHARMEL INC | CANCELLED PRE MARKET | DIN 02236965 |
| KETOPROFEN-E ECT 100MG | 100 MG | TABLET (ENTERIC-COATED) | PRO DOC LIMITEE | CANCELLED POST MARKET | DIN 02084198 |
| KETOPROFEN-E ECT 50MG | 50 MG | TABLET (ENTERIC-COATED) | PRO DOC LIMITEE | CANCELLED POST MARKET | DIN 02084171 |
| KETOPROFEN-SR - SRT 200MG | 200 MG | TABLET (EXTENDED-RELEASE) | PRO DOC LIMITEE | CANCELLED POST MARKET | DIN 02210487 |
| NOVO-KETO SUPPOSITORIES 100MG | 100 MG | SUPPOSITORY | NOVOPHARM LIMITED | CANCELLED POST MARKET | DIN 02156083 |
| NOVO-KETO-EC TAB 100MG | 100 MG | TABLET (ENTERIC-COATED) | NOVOPHARM LIMITED | CANCELLED POST MARKET | DIN 01981536 |
Who else supplies KETOPROFEN worldwide?
Nexara tracks national medicine registries and published price lists across multiple markets. KETOPROFEN appears in 47 registered pack listings across 9 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.
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.