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Cisatracurium Besylate

Cisatracurium Besylate

3 ACTIVE SUPPLIERS — US
openFDA · updated weekly
US9 NDCs
3 active makers
UKComing
soon
CAComing
soon
AUComing
soon
EUComing
soon
RxCUI (US)319864
US makers3 labelers
Packages12
DEA / ScheduleNone

Medicaid dispensing volume

No Medicaid utilization on record for this drug concept yet. Quarterly volume (CMS State Drug Utilization Data) loads with the utilization ETL.

Who makes it3 active · 0 exited

US labelers as registered with FDA. Repackagers relabel another company's product; share* is of listed packages, not sales.

LabelerTypePackagesStatus
Meitheal Pharmaceuticals Inc.unknown6SUPPLYING
Fresenius Kabi USA, LLCunknown3SUPPLYING
Hospira, Inc.unknown3SUPPLYING

Regulatory & supply eventsFDA · US

Shortages, recalls, and registration changes attached to this drug concept.

  • May 6, 2026
    RESOLVEDShortage resolved: Cisatracurium Besylate Injection (Hospira, Inc., a Pfizer Company)

    Cisatracurium Besylate Injection — reported in shortage by Hospira, Inc., a Pfizer Company. Therapeutic category: Analgesia/Addiction.

  • May 6, 2026
    SHORTAGEDrug shortage: Cisatracurium Besylate Injection (Hospira, Inc., a Pfizer Company)

    Cisatracurium Besylate Injection — reported in shortage by Hospira, Inc., a Pfizer Company. Therapeutic category: Analgesia/Addiction.

  • Jan 27, 2021
    RECALLRecall (Class I): Cisatracurium Besylate Injection, USP, 10mg per 5mL (2 mg per mL), Single-Dose Vial (NDC 71288-712-05), packaged as 10 …

    Labeling: Label mix-up: Carton of Cisatracurium Besylate Injection, USP was observed to contain ten vials mislabeled as Phenylephrine Hydrochloride Injection, USP, but confirmed to contain Cisatracurium — Recalling firm: Meitheal Pharmaceuticals Inc — Nationwide USA

  • Apr 5, 2016
    RECALLRecall (Class II): Cisatracurium Besylate Injection, 20 mg per 10 mL (2 mg per mL), For intravenous injection, 10 mL Multiple Dose Vial, R…

    Incorrect/ Undeclared Excipient: Firm is recalling product due to an incorrect statement of Preservative free on the individual carton label. The vial label and outer carton label contain the correct statement of 0.9% benzyl alcohol added as a preservative. — Recalling firm: Fresenius Kabi USA, LLC — Nationwide and Puerto Rico