PRO-NAPROXEN EC - 375 375 MG
NAPROXEN : 375 MG · DIN 02310945 · PRO DOC LIMITEE
Health Canada status: CANCELLED POST MARKET
What is PRO-NAPROXEN EC - 375?
PRO-NAPROXEN EC - 375 375 MG contains NAPROXEN : 375 MG. It is listed in the Health Canada Drug Product Database under DIN 02310945, held by PRO DOC LIMITEE, supplied as TABLET (ENTERIC-COATED) for ORAL administration. Health Canada currently lists it as cancelled post market, status dated 17-Jul-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 PRO-NAPROXEN EC - 375 used for?
Treatment of mild to moderate infections: URTI (pharyngitis/tonsillitis), LRTI (bronchitis, pneumonia), skin infections, and uncomplicated urethritis/cervicitis due to C. trachomatis.
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 | 02310945 |
|---|---|
| Brand name | PRO-NAPROXEN EC - 375 |
| Generic / active ingredient | NAPROXEN : 375 MG |
| Manufacturer | PRO DOC LIMITEE |
| Strength | 375 MG |
| Dosage form | TABLET (ENTERIC-COATED) |
| Route of administration | ORAL |
| Schedule | Prescription |
| ATC code | M01AE02 NAPROXEN |
| AHFS class | 28:08.04.92 |
| Biosimilar | No |
| Health Canada status | CANCELLED POST MARKET |
| Status date | 17-Jul-2020 |
| Original market date | 2009-10-16 00:00:00 |
How is it administered?
Adults: 500 mg as a single dose on Day 1, followed by 250 mg once daily on Days 2 through 5. For certain infections, 500 mg daily for 3 days. May be taken with or without food.
Included because it drives pack selection and wastage. Consult the monograph.
How is it stored and handled?
Store at room temperature (15°C to 30°C).
How is it supplied?
Blister packs of 6 tablets and bottles of 30 or 100 tablets.
Contraindications
Hypersensitivity to azithromycin, erythromycin, any macrolide or ketolide antibiotic, or any ingredient in the formulation. History of cholestatic jaundice/hepatic dysfunction with prior use.
Warnings and precautions
Serious allergic reactions (angioedema, anaphylaxis, Stevens-Johnson syndrome). Hepatotoxicity. Prolonged cardiac repolarization and QT interval. Clostridium difficile-associated disease.
What can be used instead?
Other Canadian products sharing ATC code M01AE02 NAPROXEN. 31 of 125 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 |
|---|---|---|---|---|---|
| ALEVE BACK AND BODY PAIN | 220 MG | CAPSULE | BAYER INC | MARKETED | DIN 02436337 |
| ALEVE CAPLETS | 220 MG | TABLET | BAYER INC | MARKETED | DIN 02301733 |
| ALEVE LIQUID GELS | 220 MG | CAPSULE | BAYER INC | MARKETED | DIN 02361795 |
| ALEVE NIGHTTIME | 220 MG | TABLET | BAYER INC | MARKETED | DIN 02444593 |
| ANAPROX | 275 MG | TABLET | SEARCHLIGHT PHARMA INC | MARKETED | DIN 02162725 |
| ANAPROX DS | 550 MG | TABLET | SEARCHLIGHT PHARMA INC | MARKETED | DIN 02162717 |
| APO-NAPRO-NA | 275 MG | TABLET | APOTEX INC | MARKETED | DIN 00784354 |
| APO-NAPRO-NA DS | 550 MG | TABLET | APOTEX INC | MARKETED | DIN 01940309 |
| APO-NAPROXEN | 250 MG | TABLET | APOTEX INC | MARKETED | DIN 00522651 |
| APO-NAPROXEN | 375 MG | TABLET | APOTEX INC | MARKETED | DIN 00600806 |
Who else supplies NAPROXEN worldwide?
Nexara tracks national medicine registries and published price lists across multiple markets. NAPROXEN appears in 1493 registered pack listings across 13 markets, published on 10 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.