APO-VORICONAZOLE 50 MG
VORICONAZOLE : 50 MG · DIN 02409674 · APOTEX INC
Health Canada status: DORMANT
Overview
APO-VORICONAZOLE 50 MG contains VORICONAZOLE : 50 MG. It is listed in the Health Canada Drug Product Database under DIN 02409674, held by APOTEX INC, supplied as TABLET for ORAL administration. Nexara Health is a licensed Canadian wholesale distributor and can source this product for hospitals, pharmacies and clinics. Availability and lead time are confirmed per order.
Product details
| DIN | 02409674 |
|---|---|
| Brand name | APO-VORICONAZOLE |
| Generic / active ingredient | VORICONAZOLE : 50 MG |
| Manufacturer | APOTEX INC |
| Strength | 50 MG |
| Dosage form | TABLET |
| Route of administration | ORAL |
| Schedule | Prescription |
| ATC code | J02AC03 VORICONAZOLE |
| AHFS class | 08:14.08 |
| Biosimilar | No |
| Health Canada status | DORMANT |
| Original market date | 2014-04-14 00:00:00 |
Indications
Invasive aspergillosis; Candidemia in non-neutropenic patients and specific Candida infections (disseminated skin, abdomen, kidney, bladder wall, and wounds).
Dosage and administration
Loading dose: 400 mg BID (Day 1); Maintenance: 200 mg BID. Adjust based on weight (<40 kg) and response. Take 1 hour before or 2 hours after meals. Halve maintenance dose in mild-moderate hepatic impairment.
Contraindications
Hypersensitivity to voriconazole; coadministration with CYP3A4 substrates (e.g., quinidine, sirolimus, pimozide, lurasidone, ivabradine, naloxegol, tolvaptan, venetoclax) or inducers (e.g., rifampin).
Warnings and precautions
Serious drug interactions; QT interval prolongation; visual disturbances; hepatic toxicity; severe cutaneous adverse reactions (SCARs); teratogenicity; and musculoskeletal (fluorosis/periostitis).
Storage and handling
Not explicitly detailed in provided text (standard section 11 was listed in TOC but text cut off), though typically 15-30°C for tablets.
Packaging
HDPE bottles of 30 tablets.
Alternatives in the same therapeutic class
Products sharing ATC code J02AC03 VORICONAZOLE. Marketed products are listed first. Substitution decisions rest with the prescriber or pharmacist, and interchangeability is determined provincially.
| Product | Manufacturer | Strength | Health Canada status | DIN |
|---|---|---|---|---|
| JAMP VORICONAZOLE | JAMP PHARMA CORPORATION | 200 MG | MARKETED | DIN 02525798 |
| JAMP VORICONAZOLE | JAMP PHARMA CORPORATION | 50 MG | MARKETED | DIN 02525771 |
| SANDOZ VORICONAZOLE | SANDOZ CANADA INCORPORATED | 50 MG | MARKETED | DIN 02399245 |
| SANDOZ VORICONAZOLE | SANDOZ CANADA INCORPORATED | 200 MG | MARKETED | DIN 02399253 |
| VFEND | PFIZER CANADA ULC | 200 MG | MARKETED | DIN 02256487 |
| VFEND | PFIZER CANADA ULC | 200 MG | MARKETED | DIN 02256479 |
| VFEND | PFIZER CANADA ULC | 200 MG / 5 ML | MARKETED | DIN 02279991 |
| VFEND | PFIZER CANADA ULC | 50 MG | MARKETED | DIN 02256460 |
Canadian availability and sourcing
Nexara Health supplies this product to licensed Canadian healthcare buyers. 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.