Doripenem

Doribax

500 MG / VIAL Powder For SolutionCanadaCancelledAuthorised 19 Oct 2009

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In other countries

The same active substances on other registers, the same brand first.

DoribaxEuropean Union · Janssen-Cilag International NVSame brand
Doribax 500MG/Vial Powder for InfusionSaudi Arabia · Shionogi & Co. LTDSame brand
DoribaxUnited States · 250MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**, 500MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · injectable · ShionogiSame brand
DoriprexBrazil · Janssen-Cilag Farmacêutica LtdaSame substance

Documents

The official texts, at the regulator.

Two medicines in one question?

Name two or more medicines and Osler runs an interaction check. A severe interaction is stated at the very top of the answer.

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Doripenem

Doribax

500 MG / VIAL Powder For SolutionCanadaCancelledAuthorised 19 Oct 2009

Open in the registerAsk Osler about it

This page is kept for reference and is not offered to search engines.

In other countries

The same active substances on other registers, the same brand first.

Documents

The official texts, at the regulator.

Two medicines in one question?

Name two or more medicines and Osler runs an interaction check. A severe interaction is stated at the very top of the answer.

Discover Osler

Register entryHealth Canada

Sources and licences

Compiled by Prognia from the public register below; the register’s text is the official one.

Health Canada, Canada

Health Canada, Drug Product Database, drugproduct API, entire response observed 2026-10-10T15:12:07.336870+00:00; native facts projected by Prognia.

Licence: Open Government Licence Canada · Added 13 Oct 2026

Report an error or request removalCorrections from the holder or the register are welcome.

Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.

At a glance

Active substance: Doripenem
Strength: 500 MG / VIAL
Dosage form: Powder For Solution
Route: Intravenous
Register: Canada (Health Canada)
Status: Cancelled
Status in the register: Cancelled Post Market
Authorised: 19 Oct 2009
Registration: DIN 02332906
Marketing authorisation holder: Janssen INC
ATC code: J01DH04
Group: Anti-infectives for systemic use
Supply: PRESCRIPTION