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Last Updated: March 29, 2024

ATRACURIUM BESYLATE PRESERVATIVE FREE Drug Patent Profile


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Which patents cover Atracurium Besylate Preservative Free, and what generic alternatives are available?

Atracurium Besylate Preservative Free is a drug marketed by Baxter Hlthcare, Baxter Hlthcare Corp, Eugia Pharma, Hikma, Hospira, Hospira Inc, Meitheal, Mylan Labs Ltd, and Watson Labs Inc. and is included in eleven NDAs.

The generic ingredient in ATRACURIUM BESYLATE PRESERVATIVE FREE is atracurium besylate. There are sixteen drug master file entries for this compound. Three suppliers are listed for this compound. Additional details are available on the atracurium besylate profile page.

DrugPatentWatch® Litigation and Generic Entry Outlook for Atracurium Besylate Preservative Free

A generic version of ATRACURIUM BESYLATE PRESERVATIVE FREE was approved as atracurium besylate by HIKMA on July 18th, 1997.

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Drug patent expirations by year for ATRACURIUM BESYLATE PRESERVATIVE FREE
Pharmacology for ATRACURIUM BESYLATE PRESERVATIVE FREE
Anatomical Therapeutic Chemical (ATC) Classes for ATRACURIUM BESYLATE PRESERVATIVE FREE

US Patents and Regulatory Information for ATRACURIUM BESYLATE PRESERVATIVE FREE

Applicant Tradename Generic Name Dosage NDA Approval Date TE Type RLD RS Patent No. Patent Expiration Product Substance Delist Req. Exclusivity Expiration
Baxter Hlthcare ATRACURIUM BESYLATE PRESERVATIVE FREE atracurium besylate INJECTABLE;INJECTION 074825-001 Sep 30, 1997 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Hospira ATRACURIUM BESYLATE PRESERVATIVE FREE atracurium besylate INJECTABLE;INJECTION 074741-001 Mar 28, 1997 DISCN No No ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Hikma ATRACURIUM BESYLATE PRESERVATIVE FREE atracurium besylate INJECTABLE;INJECTION 074900-001 Jul 18, 1997 AP RX No Yes ⤷  Try a Trial ⤷  Try a Trial ⤷  Try a Trial
Hospira Inc ATRACURIUM BESYLATE PRESERVATIVE FREE atracurium besylate INJECTABLE;INJECTION 090782-001 Oct 18, 2012 AP RX 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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