Pentostatin

Nipent PWS 10MG/Vial

10 MG / VIAL Powder For SolutionCanadaCancelledAuthorised 31 Dec 1993

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In other countries

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

NIPENT 10 mg POLVO PARA SOLUCION INYECTABLE Y PARA PERFUSIONSpain · 10,0 mg · polvo para solución inyectable y para perfusión · Pfizer S.L.Same brand
NipentItaly · Polvere per soluzione iniettabile · Pfizer Italia S.R.L.Same brand
NipentNew Zealand · Inj 10 mgSame brand
NipentUnited States · 10MG/VIAL · injectable · Hospira INCSame brand
PentostatinUnited States · 10MG/VIAL · injectable · RisingSame substance

Documents

The official texts, at the regulator.

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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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Pentostatin

Nipent PWS 10MG/Vial

10 MG / VIAL Powder For SolutionCanadaCancelledAuthorised 31 Dec 1993

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: Pentostatin
Strength: 10 MG / VIAL
Dosage form: Powder For Solution
Route: Intravenous
Register: Canada (Health Canada)
Status: Cancelled
Status in the register: Cancelled Post Market
Authorised: 31 Dec 1993
Registration: DIN 02011247
Marketing authorisation holder: Parke-Davis Division, Warner-Lambert Canada INC.
ATC code: L01XX08
Group: Antineoplastic and immunomodulating agents
Supply: PRESCRIPTION