PMS-FENOFIBRATE SUPRA 100 MG
FENOFIBRATE : 100 MG · DIN 02251728 · PHARMASCIENCE INC
Health Canada status: APPROVED
What is PMS-FENOFIBRATE SUPRA?
PMS-FENOFIBRATE SUPRA 100 MG contains FENOFIBRATE : 100 MG. It is listed in the Health Canada Drug Product Database under DIN 02251728, held by PHARMASCIENCE INC, supplied as TABLET for ORAL administration. Health Canada currently lists it as approved, status dated 12-Jan-2005. 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 | 02251728 |
|---|---|
| Brand name | PMS-FENOFIBRATE SUPRA |
| Generic / active ingredient | FENOFIBRATE : 100 MG |
| Manufacturer | PHARMASCIENCE INC |
| Strength | 100 MG |
| Dosage form | TABLET |
| Route of administration | ORAL |
| Schedule | Prescription |
| ATC code | C10AB05 FENOFIBRATE |
| AHFS class | 24:06.06 |
| Biosimilar | No |
| Health Canada status | APPROVED |
| Status date | 12-Jan-2005 |
What can be used instead?
Other Canadian products sharing ATC code C10AB05 FENOFIBRATE. 10 of 56 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 |
|---|---|---|---|---|---|
| AA-FENO-MICRO | 200 MG | CAPSULE | AA PHARMA INC | MARKETED | DIN 02239864 |
| AA-FENO-MICRO | 67 MG | CAPSULE | AA PHARMA INC | MARKETED | DIN 02243180 |
| AA-FENO-SUPER | 100 MG | TABLET | AA PHARMA INC | MARKETED | DIN 02246859 |
| AA-FENO-SUPER | 160 MG | TABLET | AA PHARMA INC | MARKETED | DIN 02246860 |
| LIPIDIL EZ | 145 MG | TABLET | BGP PHARMA ULC | MARKETED | DIN 02269082 |
| LIPIDIL EZ | 48 MG | TABLET | BGP PHARMA ULC | MARKETED | DIN 02269074 |
| LIPIDIL SUPRA | 160 MG | TABLET | BGP PHARMA ULC | MARKETED | DIN 02241602 |
| SANDOZ FENOFIBRATE E | 145.0 MG | TABLET | SANDOZ CANADA INCORPORATED | MARKETED | DIN 02390701 |
| SANDOZ FENOFIBRATE E | 48.0 MG | TABLET | SANDOZ CANADA INCORPORATED | MARKETED | DIN 02390698 |
| SN-FENOFIBRATE E | 145 MG | TABLET | SUN PHARMA CANADA INC | MARKETED | DIN 02454696 |
Who else supplies FENOFIBRATE worldwide?
Nexara tracks national medicine registries and published price lists across multiple markets. FENOFIBRATE appears in 412 registered pack listings across 12 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?
This product is approved by Health Canada but not yet marketed in Canada, so there is no Canadian supply to draw on today. Nexara can tell you whether it has been launched, and can look at supply from other markets where a Canadian pack is not required or where importation is 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.