MedPath

Vinblastine

Generic Name
Vinblastine
Drug Type
Small Molecule
Chemical Formula
C46H58N4O9
CAS Number
865-21-4
Unique Ingredient Identifier
5V9KLZ54CY

Overview

Antitumor alkaloid isolated from Vinca rosea. (Merck, 11th ed.)

Indication

For treatment of breast cancer, testicular cancer, lymphomas, neuroblastoma, Hodgkin's and non-Hodgkin's lymphomas, mycosis fungoides, histiocytosis, and Kaposi's sarcoma.

Associated Conditions

  • Advanced Soft Tissue Sarcoma
  • Autoimmune Hemolytic Anemia
  • Bladder Cancer
  • Hodgkin's Lymphoma
  • Immune Thrombocytopenia (ITP)
  • Kaposi's Sarcoma
  • Letterer-Siwe disease
  • Metastatic Melanoma
  • Non-Small Cell Lung Cancer (NSCLC)
  • Advanced Alibert-Bazin syndrome
  • Advanced Testicular cancer
  • Histiocytic lymphoma
  • Refractory Breast cancer

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2025/05/22
Phase 2
Recruiting
National Medical Research Radiological Centre of the Ministry of Health of Russia
2025/05/07
Phase 3
Recruiting
2025/02/18
Phase 4
Recruiting
2024/12/20
Phase 2
Recruiting
2024/04/24
Early Phase 1
Recruiting
Daniel Morgenstern
2024/04/22
Phase 2
Recruiting
2024/01/12
Early Phase 1
Not yet recruiting
2023/12/11
Phase 2
Active, not recruiting
2023/01/09
Phase 3
Recruiting
2022/06/03
Phase 2
Recruiting

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Fresenius Kabi USA, LLC
63323-278
INTRAVENOUS
1 mg in 1 mL
12/31/2019

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
DBL™ VINBLASTINE INJECTION
SIN07944P
INJECTION
1 mg/ml
12/9/1994
VELBASTINE FOR INJECTION 10 mg/vial
SIN10987P
INJECTION, POWDER, FOR SOLUTION
10 mg/vial
6/24/1999

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
VINBLASTINE SULFATE INJECTION
02183056
Solution - Intravenous
1 MG / ML
4/14/1998
VINBLASTINE SULFATE INJECTION
02406675
Solution - Intravenous
1 MG / ML
N/A
VELBE 1MG/ML
eli lilly canada inc
00015431
Powder For Solution - Intravenous
10 MG / 10 ML
11/15/1994
VINBLASTINE SULFATE INJ 1MG/ML
david bull laboratories (pty) ltd.
01977784
Liquid - Intravenous
1 MG / ML
12/31/1992
VINBLASTINE SULPHATE INJECTION
teva canada limited
02401460
Solution - Intravenous
1 MG / ML
2/8/2013

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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