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Medicines · US (FDA)

FDA 2003

Vinca alkaloids and analogues

Vincristine Sulfate

Approved 28 Oct 2003InjectionInjectable

The FDA lists this product in 12 strengths and forms.

Official labelAsk Osler about it

On this page

Composition
Strengths and forms
Official product information

The table holds no label text for this product yet, only the facts beside it. The official product information has the full text.

Composition

Active ingredients: VINCRISTINE SULFATE 1MG/ML

Strengths and forms

The FDA lists each strength of a product separately; these pages share one label.

VINCRISTINE SULFATE 1MG/ML · InjectableThis page
VINCRISTINE SULFATE 5MG/VIAL · InjectableANDA071561-001 · Discontinued
VINCRISTINE SULFATE 1MG/ML · InjectableANDA070777-001 · Discontinued
VINCRISTINE SULFATE 5MG/VIAL · InjectableANDA071937-001 · Discontinued
VINCRISTINE SULFATE 1MG/VIAL · InjectableANDA071222-001 · Discontinued
VINCRISTINE SULFATE 2MG/VIAL · InjectableANDA071560-001 · Discontinued
VINCRISTINE SULFATE 1MG/ML · InjectableANDA070873-001 · Discontinued
VINCRISTINE SULFATE 1MG/VIAL · InjectableANDA071559-001 · Discontinued
VINCRISTINE SULFATE 1MG/ML · InjectableANDA076296-001 · Discontinued
VINCRISTINE SULFATE 1MG/ML · InjectableANDA070411-001 · Discontinued

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.

VINCRISTINE SULFATE 2MG/VIAL · InjectableANDA071223-001 · Discontinued

VINCRISTINE SULFATE 1MG/ML · InjectableANDA070778-001 · Discontinued

Official product information

Drugs@FDA lists the approved labels, letters and reviews for application ANDA076401.

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

Brand name: Vincristine Sulfate
Drug class: Vinca alkaloids and analogues
Route: Injection
Dosage form: Injectable
Applicant: Fresenius Kabi USA
Status: Discontinued
FDA approval: 28 Oct 2003
Application: ANDA076401-001
RxCUI: 11203