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Last Updated: April 19, 2024

VINBLASTINE SULFATE Drug Patent Profile


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When do Vinblastine Sulfate patents expire, and when can generic versions of Vinblastine Sulfate launch?

Vinblastine Sulfate is a drug marketed by Abraxis Pharm, Fresenius Kabi Usa, Hikma, and Hospira. and is included in four NDAs.

The generic ingredient in VINBLASTINE SULFATE is vinblastine sulfate. There are seven drug master file entries for this compound. One supplier is listed for this compound. Additional details are available on the vinblastine sulfate profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Vinblastine Sulfate

A generic version of VINBLASTINE SULFATE was approved as vinblastine sulfate by HIKMA on April 9th, 1987.

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Drug patent expirations by year for VINBLASTINE SULFATE
Recent Clinical Trials for VINBLASTINE SULFATE

Identify potential brand extensions & 505(b)(2) entrants

SponsorPhase
Hospital Universitario Dr. Jose E. GonzalezPhase 2
University of WashingtonPhase 2
AstraZenecaPhase 2

See all VINBLASTINE SULFATE clinical trials

Pharmacology for VINBLASTINE SULFATE
Drug ClassVinca Alkaloid
Medical Subject Heading (MeSH) Categories for VINBLASTINE SULFATE

US Patents and Regulatory Information for VINBLASTINE SULFATE

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Abraxis Pharm VINBLASTINE SULFATE vinblastine sulfate INJECTABLE;INJECTION 089011-001 Nov 18, 1985 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Hospira VINBLASTINE SULFATE vinblastine sulfate INJECTABLE;INJECTION 089565-001 Aug 18, 1987 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Fresenius Kabi Usa VINBLASTINE SULFATE vinblastine sulfate INJECTABLE;INJECTION 089515-001 Apr 29, 1987 RX No Yes ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Hikma VINBLASTINE SULFATE vinblastine sulfate INJECTABLE;INJECTION 089395-001 Apr 9, 1987 RX No Yes ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
>Applicant >Tradename >Generic Name >Dosage >NDA >Approval Date >TE >Type >RLD >RS >Patent No. >Patent Expiration >Product >Substance >Delist Req. >Exclusivity Expiration

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