Burrard Pharmaceuticals Enterprises Ltd., Vancouver, Canada, supports importers, distributors, and local marketing-authorisation holders seeking sertraline finished-dose supply through a partner-site model.
Email bd@burrardpharma.com with your company, territory, and finished-dose supply, dossier support, or both.
Burrard does not manufacture in-house. Manufacture for this programme is placed with a qualified partner GMP site named under CDA.
Site GMP evidence is shared in the quality pack under CDA. Site GMP is not product approval.
This page discusses the INN sertraline. Zoloft is named for identification only and is not a Burrard trademark or a Burrard-branded good.
Sertraline is a selective serotonin reuptake inhibitor in the established oral class.
Oral solid, strengths confirmed under CDA.
Other medicines in the same class, oral concentrate, and salts not named on this page are out of scope unless separately confirmed under CDA.
These requests are still business-to-business. Send company, territory, and finished-dose supply, dossier support, or both. Do not send patient histories. Salt is confirmed under CDA.
Scope table. Public copy only. Strengths, packs, stability, and dossier status are confirmed under CDA, not on this page.
| INN | Sertraline |
| Dosage form | Oral solid, strengths confirmed under CDA |
| Strengths | Confirmed under CDA / quality pack |
| Pack sizes | Confirmed under CDA / quality pack |
| Stability / climate zone | Not stated. Confirmed under CDA. |
| Dossier format | Not asserted. Confirmed under CDA if a file is offered. |
| Facility class | Named site, in the quality pack. |
| WHO prequalification | Not claimed |
| Bioequivalence | Not claimed |
| MOQ / Incoterms | Confirmed under CDA |
| Exclusivity note | US tablet compound patent, with paediatric exclusivity, expired 30 June 2006. Later patents on other presentations are not cleared here. |
Burrard coordinates sertraline finished-dose supply for commercial partners. Manufacture is at a qualified partner GMP site named under CDA, not at a Burrard plant. The reader is a partner, not a patient. This page is not a dose and not a superiority claim. Price and pack count are not published. The order of work is the quality pack, then site and batch evidence under CDA, then a short supply call.
The pack is a B2B qualification file. It is not a marketing authorisation and not a patient leaflet.
GMP or API documents describe the named site or the API. They are not Burrard product approval in the United States, the European Union, Canada, or elsewhere. This page claims no FDA, EMA, or Health Canada product approval and no country-of-origin marketing authorisation. The local MAH or importer holds the destination authorisation.
The US compound patent on the originator tablets, with paediatric exclusivity, expired on 30 June 2006. That is the date generic sertraline tablets entered ordinary US commerce. Sertraline is a long off-patent generic for that tablet history. This page does not clear later patents on other presentations. Oral concentrate is out of scope. Not every country is claimed open.
Burrard discusses supply only where relevant exclusivity has ended. Zoloft is an originator name for identification only, not a Burrard trademark. The class sentence is not a patient claim and not dosing advice.
Burrard does not quote a molecule under a live patent or exclusivity dispute in the requested territory. Supply is discussed only where relevant exclusivity has ended.
Each link is a separate finished-dose programme with its own exclusivity note. Escitalopram.
No. Burrard does not manufacture in-house. Manufacture is placed with a qualified partner GMP site named under CDA. The site is named in the quality pack after CDA.
No. This page does not claim FDA, EMA, or Health Canada product approval for sertraline. The local MAH or importer holds destination marketing authorisation. Site GMP evidence is not product approval.
Oral solid, strengths confirmed under CDA. Pack size, stability zone, and CTD or ACTD status are not stated here.
No. The date on this page is 30 June 2006 for the US tablet compound patent with paediatric exclusivity. Oral concentrate and other presentations are out of scope unless separately confirmed under CDA. Not every country is claimed open. Supply is discussed only where relevant exclusivity has ended.
Email bd@burrardpharma.com with your company, territory, and whether you need finished-dose supply, dossier support, or both. The quality pack and a short supply call follow CDA.
Email bd@burrardpharma.com with company, territory, and finished-dose supply, dossier support, or both. You can also use the contact page.
For importers, distributors, and local marketing-authorisation holders only. Not patient information, not dosing guidance, and not an offer or a price. Burrard Pharmaceuticals Enterprises Ltd. does not manufacture in-house and does not claim FDA, EMA, or Health Canada product approval. Site GMP is not product approval. The local MAH or importer holds destination authorisation. Supply is discussed only where relevant exclusivity has ended. Strengths, packs, stability zones, and CTD status are confirmed under CDA, not here. Brand names are for identification only.