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Last Updated: March 29, 2024

Droperidol - Generic Drug Details


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What are the generic sources for droperidol and what is the scope of freedom to operate?

Droperidol is the generic ingredient in four branded drugs marketed by Abraxis Pharm, Am Regent, Astrazeneca, Hikma, Hospira, Igi Labs Inc, Luitpold, Smith And Nephew, Solopak, Watson Labs, Rising, and Epic Pharma Llc, and is included in twenty-four NDAs. Additional information is available in the individual branded drug profile pages.

There are five drug master file entries for droperidol. Two suppliers are listed for this compound.

Summary for droperidol
Recent Clinical Trials for droperidol

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

SponsorPhase
RenJi HospitalN/A
Mercy Health OhioPhase 3
Lake Erie College of Osteopathic MedicinePhase 3

See all droperidol clinical trials

Pharmacology for droperidol
Medical Subject Heading (MeSH) Categories for droperidol

US Patents and Regulatory Information for droperidol

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Solopak DROPERIDOL droperidol INJECTABLE;INJECTION 071754-001 Sep 6, 1988 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Rising INAPSINE droperidol INJECTABLE;INJECTION 016796-001 Approved Prior to Jan 1, 1982 DISCN Yes No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Igi Labs Inc DROPERIDOL droperidol INJECTABLE;INJECTION 072021-001 Oct 19, 1988 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Igi Labs Inc DROPERIDOL droperidol INJECTABLE;INJECTION 072019-001 Oct 19, 1988 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Epic Pharma Llc INNOVAR droperidol; fentanyl citrate INJECTABLE;INJECTION 016049-001 Approved Prior to Jan 1, 1982 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Abraxis Pharm DROPERIDOL droperidol INJECTABLE;INJECTION 070992-001 Nov 17, 1986 DISCN No No ⤷  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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