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Prescription medicine

Succinylcholine Brand names: Anectine, Quelicin

Succinylcholine (Anectine) is a prescription medicine with an FDA approval on record since 1952. FDA's NDC Directory lists it from 26 generic labelers.

  • Generic listed
  • A presentation discontinued
  • Boxed warning

Check it at the source: the succinylcholine FDA label on DailyMed (effective August 18, 2026, Hospira, Inc.); the NDA 8453 record on Drugs@FDA; every succinylcholine label on DailyMed.

Highlights of the record

FDA label of August 18, 2026; NDC Directory, Drugs@FDA and Orange Book, October 8, 2026

Boxed warning

VENTRICULAR DYSRHYTHMIAS, CARDIAC ARREST, AND DEATH FROM HYPERKALEMIC RHABDOMYOLYSIS IN PEDIATRIC PATIENTS •.

Acute rhabdomyolysis with hyperkalemia followed by ventricular dysrhythmias, cardiac arrest, and death has occurred after the administration of succinylcholine to apparently healthy pediatric patients who were subsequently found to have undiagnosed skeletal muscle myopathy, most frequently Duchenne muscular dystrophy [see Warnings and Precautions (5.1) ].

When a healthy appearing pediatric patient develops cardiac arrest within minutes after administration of QUELICIN, not felt to be due to inadequate ventilation, oxygenation or anesthetic overdose, immediate treatment for hyperkalemia should be instituted. In the presence of signs of malignant hyperthermia, appropriate treatment should be instituted concurrently [see Warnings and Precautions (5.1) ].

Reserve the use of QUELICIN in pediatric patients for emergency intubation or instances where immediate securing of the airway is necessary, e.g., laryngospasm, difficult airway, full stomach, or for intramuscular use when a suitable vein is inaccessible [see Warnings and Precautions (5.1) ]. WARNING: VENTRICULAR DYSRHYTHMIAS, CARDIAC ARREST, AND DEATH FROM HYPERKALEMIC RHABDOMYOLYSIS IN PEDIATRIC PATIENTS See full prescribing information for complete boxed warning. […]

Used for

From the label: indications and usage

QUELICIN is indicated in adults and pediatric patients:

as an adjunct to general anesthesia

to facilitate tracheal intubation

to provide skeletal muscle relaxation during surgery or mechanical ventilation.

Forms and strengths

  • 20 mg/ml
  • 200 mg/10ml

Injection (solution); injection.

On the market

Earliest approval on file
August 20, 1952 Anectine, Sandoz; Drugs@FDA’s file, where older or withdrawn approvals can be missing
Generic approvals
28 first September 20, 1972; 20 with a marketed status in Drugs@FDA
Labelers listed (NDC)
29 of which 26 under generic applications, 3 under brand applications, repackagers included
Last listed patent
November 2, 2041 Succinylcholine Chloride injection; not a generic launch date

Supply and safety

Pharmacy cost (NADAC)
Not in the survey
Shortage (FDA)
None current 1 past records
Recalls by its makers (FDA)
30 since 2013 0 Class I among all firms' recalls; latest September 26, 2025; 9 more by firms not listed as its makers
FAERS reports
3,844 through July 30, 2026

What is succinylcholine used for?

From the label: indications and usage

QUELICIN is indicated in adults and pediatric patients:

as an adjunct to general anesthesia

to facilitate tracheal intubation

to provide skeletal muscle relaxation during surgery or mechanical ventilation. QUELICIN is a depolarizing neuromuscular blocker indicated in adults and pediatric patients:

as an adjunct to general anesthesia ( 1 )

to facilitate tracheal intubation ( 1 )

to provide skeletal muscle relaxation during surgery or mechanical ventilation.

FDA pharmacologic class: Depolarizing Neuromuscular Blocker.

Source: FDA drug label (QUELICIN), Hospira, Inc., effective August 18, 2026 (SPL set fb08161e-7711-406d-e7b3-ea4515c07983), via openFDA; the full label on DailyMed

Is there a generic for succinylcholine (Anectine)?

The FDA approved the first generic succinylcholine on September 20, 1972. 28 generic applications are approved; 20 of them carry a current (not discontinued) marketing status in Drugs@FDA; that status is not evidence that the generic is on sale.

FDA's NDC Directory lists succinylcholine from 26 labelers under a generic (ANDA) application and from 3 brand labelers. A listing means the company has registered the product for sale; it does not show that every pharmacy stocks it.

The Orange Book lists no patent for Anectine injection; a patent listed only for Succinylcholine Chloride injection runs to November 2, 2041. A patent or exclusivity date is not the date a generic goes on sale: court cases and settlements move it either way.

  • 1952 earliest approval on file
  • 1972 first generic approved
  • 2041 last listed patent
  • red ticks recalls

Source: Drugs@FDA, FDA NDC Directory and the Orange Book (openFDA bulk files, October 8, 2026)

Is succinylcholine in shortage?

No succinylcholine presentation is listed as in shortage in the FDA Drug Shortage Database (read October 8, 2026); its 1 record is all marked to be discontinued, the latest updated July 23, 2026. ASHP keeps a separate shortage list, which can differ.

PresentationCompanyStatusUpdated
Succinylcholine Chloride, Injection, 20 mg/1 mL (NDC 63323-943-10)Fresenius Kabi USA, LLCTo Be DiscontinuedJuly 23, 2026

Every succinylcholine presentation in the FDA shortage database

Source: FDA Drug Shortage Database via openFDA, updated October 8, 2026

Has succinylcholine been recalled?

The FDA's Enforcement Report lists 39 recalls naming succinylcholine since 2013: 0 Class I (the most serious), 38 Class II, 1 Class III; 3 still ongoing. 9 of them are by firms that FDA's NDC Directory does not list as a maker of succinylcholine and that hold no application for it in Drugs@FDA, such as compounding pharmacies or bulk-ingredient suppliers; the recall notice names the product recalled. A recall names products and lots, not every product of the medicine.

StartedClassCompanyReason
September 26, 2025Class IIDr. Reddy's Laboratories, Inc.Out-of-Specification (OOS) result during the 6-month stability testing; decreased preservative concentration.
August 27, 2025Class IIZydus Pharmaceuticals (USA) IncFailed Impurities/Degradation Specifications: Out-of-Specification test results obtained for any individual unknown degradation impurity.
November 9, 2023Class IISCA Pharmaceuticals, LLCLack of Assurance of Sterility
September 21, 2023Class IICentral Admixture Pharmacy Services IncLack of assurance of sterility:
July 17, 2023Class IICentral Admixture Pharmacy Services IncLack of assurance of sterility: Lack of validation data for sanitization cycles
July 14, 2023Class IICentral Admixture Pharmacy Services, Inc.Lack of assurance of sterility. Validation data for decontamination cycles is lacking.
July 10, 2023Class IINew England Life Care, Inc. dba Advanced Compounding … not a listed makerCGMP Violations- that spaces adjacent to the production area may have been compromised at the time of production.
February 7, 2023Class IIAccord Healthcare, Inc.CGMP Deviations: recalling drug products following an FDA inspection.

Source: FDA Enforcement Report (drug recalls) via openFDA, through October 8, 2026

What does the succinylcholine label say about other medicines?

The succinylcholine label names 13 other medicines in its interaction, contraindication or warning sections. The labels of 33 other medicines name succinylcholine. The sentences are the labels' own; a label lists what its studies and reports found, not every interaction.

Medicine namedSectionWhat the label says
Atropinewarnings and precautionsPretreatment with anticholinergic agents (e.g., atropine) may reduce the occurrence of bradyarrhythmias.
Chloroquinedrug interactions… β-adrenergic blockers, procainamide, lidocaine, trimethaphan, lithium carbonate, magnesium salts, quinine, chloroquine, isoflurane, desflurane, metoclopramide, terbutaline, and drugs that reduce plasma cholinesterase activity.
Dantrolenewarnings and precautionsMalignant Hyperthermia: Malignant hyperthermia may occur, especially in individuals with known or suspected susceptibility based on genetic factors or family history. Discontinue triggering agents, administer intravenous dantrolene sodium, and apply supportive therapies.
Desfluranedrug interactions… procainamide, lidocaine, trimethaphan, lithium carbonate, magnesium salts, quinine, chloroquine, isoflurane, desflurane, metoclopramide, terbutaline, and drugs that reduce plasma cholinesterase activity.
Echothiophatewarnings and precautionsPlasma cholinesterase activity may also be diminished by chronic administration of oral contraceptives, glucocorticoids, or certain monoamine oxidase inhibitors and by irreversible inhibitors of plasma cholinesterase (e.g., organophosphate insecticides, echothiophate, and certain antineoplastic drugs) [see Drug …
Isofluranedrug interactions… blockers, procainamide, lidocaine, trimethaphan, lithium carbonate, magnesium salts, quinine, chloroquine, isoflurane, desflurane, metoclopramide, terbutaline, and drugs that reduce plasma cholinesterase activity.
Lidocainedrug interactionsDRUG INTERACTIONS Drugs that May Enhance the Neuromuscular Blocking Action of Succinylcholine: promazine, oxytocin, aprotinin, certain non-penicillin antibiotics, quinidine, β-adrenergic blockers, procainamide, lidocaine, trimethaphan, lithium carbonate, magnesium salts, quinine, chloroquine, isoflurane, desflurane …
Lithiumdrug interactionsDRUG INTERACTIONS Drugs that May Enhance the Neuromuscular Blocking Action of Succinylcholine: promazine, oxytocin, aprotinin, certain non-penicillin antibiotics, quinidine, β-adrenergic blockers, procainamide, lidocaine, trimethaphan, lithium carbonate, magnesium salts, quinine, chloroquine, isoflurane, desflurane …
Metoclopramidedrug interactions… lidocaine, trimethaphan, lithium carbonate, magnesium salts, quinine, chloroquine, isoflurane, desflurane, metoclopramide, terbutaline, and drugs that reduce plasma cholinesterase activity.
Procainamidedrug interactionsDRUG INTERACTIONS Drugs that May Enhance the Neuromuscular Blocking Action of Succinylcholine: promazine, oxytocin, aprotinin, certain non-penicillin antibiotics, quinidine, β-adrenergic blockers, procainamide, lidocaine, trimethaphan, lithium carbonate, magnesium salts, quinine, chloroquine, isoflurane, desflurane …
Quinidinedrug interactionsDRUG INTERACTIONS Drugs that May Enhance the Neuromuscular Blocking Action of Succinylcholine: promazine, oxytocin, aprotinin, certain non-penicillin antibiotics, quinidine, β-adrenergic blockers, procainamide, lidocaine, trimethaphan, lithium carbonate, magnesium salts, quinine, chloroquine, isoflurane, desflurane …
Quininedrug interactionsDRUG INTERACTIONS Drugs that May Enhance the Neuromuscular Blocking Action of Succinylcholine: promazine, oxytocin, aprotinin, certain non-penicillin antibiotics, quinidine, β-adrenergic blockers, procainamide, lidocaine, trimethaphan, lithium carbonate, magnesium salts, quinine, chloroquine, isoflurane, desflurane …
Terbutalinedrug interactions… trimethaphan, lithium carbonate, magnesium salts, quinine, chloroquine, isoflurane, desflurane, metoclopramide, terbutaline, and drugs that reduce plasma cholinesterase activity.

Other labels that name succinylcholine

Check succinylcholine against other medicines

Source: FDA drug label (QUELICIN), Hospira, Inc., effective August 18, 2026 (SPL set fb08161e-7711-406d-e7b3-ea4515c07983), via openFDA; the full label on DailyMed

What do FAERS reports show for succinylcholine?

The FDA Adverse Event Reporting System holds 3,844 reports that list succinylcholine among the medicines taken, through July 30, 2026, each a report of something that happened, not proof the medicine caused it; 390 are coded as a death and 1,395 as a hospital stay. Counts follow how widely a medicine is used and watched, and they are not a measure of how risky it is.

Reports received each year

The most reported reactions

  • Drug Ineffective (a use or a product term, not a reaction)443
  • Hypotension (named in the label)310
  • Hyperthermia Malignant287
  • Cardiac Arrest (named in the label)260
  • Drug Interaction (a use or a product term, not a reaction)225
  • Anaphylactic Shock220
  • Anaphylactic Reaction (named in the label)184
  • Pain139

Side effects: the label's list and every FAERS reaction

Source: FDA Adverse Event Reporting System (FAERS) via openFDA, reports through July 30, 2026

What next?

Succinylcholine side effects
the label's list beside FAERS reports
Succinylcholine shortage record
every presentation, company and date
Check an interaction
what two or more labels say about each other