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Approved Drug Products containing Vinblastine listed in the FDA Orange Book. Original Data : FDA Website

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01 1ABRAXIS PHARM

02 1FRESENIUS KABI USA

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04 1HOSPIRA

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06 2QUAD PHARMS

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PharmaCompass

01

Pharmaconex 2024
Not Confirmed
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Pharmaconex 2024
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VINBLASTINE SULFATE

Brand Name : VINBLASTINE SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 10MG/VIAL

Approval Date : 1985-11-18

Application Number : 89011

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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02

Pharmaconex 2024
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Pharmaconex 2024
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VINBLASTINE SULFATE

Brand Name : VELBAN

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 10MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 12665

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

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03

Pharmaconex 2024
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Pharmaconex 2024
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VINBLASTINE SULFATE

Brand Name : VINBLASTINE SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 1MG/ML

Approval Date : 1987-04-29

Application Number : 89515

RX/OTC/DISCN : RX

RLD : No

TE Code :

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04

Pharmaconex 2024
Not Confirmed
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Pharmaconex 2024
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VINBLASTINE SULFATE

Brand Name : VINBLASTINE SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 10MG/VIAL

Approval Date : 1987-04-09

Application Number : 89395

RX/OTC/DISCN : RX

RLD : No

TE Code :

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05

Pharmaconex 2024
Not Confirmed
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Pharmaconex 2024
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VINBLASTINE SULFATE

Brand Name : VINBLASTINE SULFATE

Dosage Form : INJECTABLE;INJECTION

Dosage Strength : 10MG/VIAL

Approval Date : 1987-08-18

Application Number : 89565

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

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06

Pharmaconex 2024
Not Confirmed
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Pharmaconex 2024
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VINBLASTINE SULFATE

Brand Name : VINBLASTINE SULFATE

Dosage Form : Injectable; Injection

Dosage Strength : 1MG/ML

Approval Date :

Application Number : 89311

RX/OTC/DISCN :

RLD :

TE Code :

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07

Pharmaconex 2024
Not Confirmed
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Pharmaconex 2024
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VINBLASTINE SULFATE

Brand Name : VINBLASTINE SULFATE

Dosage Form : Injectable; Injection

Dosage Strength : 10MG/VIAL

Approval Date :

Application Number : 89365

RX/OTC/DISCN :

RLD :

TE Code :

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