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Medicine

Anectine 200 mg/10 mL injection

Succinylcholine · Intramuscular, intravenous, parenteral · Sandoz
Available on requestPrescription onlyUS FDA Cold chain

Anectine 200 mg/10 mL injection is a prescription medicine containing Succinylcholine for intramuscular, intravenous, parenteral use, marketed by Sandoz, with its source record on the US FDA register. It is available on request for export supply from India to licensed hospitals, importers and physicians. It ships in a temperature-controlled cold chain.

Availability

Available on request

Export supply from India to licensed buyers

Typical lead time

On request

Counted from payment and complete documents

Shipping

Cold chain

Store in refrigerator at 2° to 8°C (36° to 46°F). The multi-dose vials are…

Key facts

Active ingredient (INN)
Succinylcholine
Brand
Anectine
Strength
200 mg/10 mL
Dosage form
Injection
Route
Intramuscular, intravenous, parenteral
Packs
10 vials of 10 mL
Marketing authorisation holder
Sandoz
Manufacturers
SandozCivica
Origin register
US FDA, United States
Storage
Store in refrigerator at 2° to 8°C (36° to 46°F). The multi-dose vials are stable for up to 14 days at room temperature without significant loss of potency.
Cold chain
Yes, shipped temperature controlled
Prescription status
Prescription only
Controlled substance
Not recorded as controlled
ATC code
M03AB01 Succinylcholine
HS code (indicative)
3004.90Indicative only. Your customs broker confirms the final tariff code.
Marketing category
marketed
Marketed since
22 June 2017
Identifiers
RxCUI 1594589, 1594591DailyMed set ID a1e5d29f-111e-4a44-addf-beeb6ea81711, 04a4e6f5-6fa1-42e1-a3f9-21fca7786b15, 0b990f84-9515-44bd-a97d-a97bbead065cNDC 0781-3411, 0781-9053, 72572-750Application NDA008453

Record updated 12 November 2026

Documents available

Documents that can be provided with this medicine. Your regulator may ask for more, and the quote lists the full set.

No document list is recorded for this medicine yet. Tell us which documents your regulator needs (for example a CoA, COPP or GMP certificate) when you request a quote.

Packs

PackCodeLabelerMarketed since
10 vial, multi-dose in 1 carton / 10 mL in 1 vial, multi-dose0781-3411-95Sandoz22 June 2017
10 vial, multi-dose in 1 carton / 10 mL in 1 vial, multi-dose0781-9053-95Sandoz12 June 2019
10 vial, multi-dose in 1 carton / 10 mL in 1 vial, multi-dose72572-750-10Civica11 December 2020

Status by register

Where this medicine is registered, from the source record and the regulator data we hold. Ask us about a country that is not listed.

RegisterStatusSource
US FDAListed, marketedSource record for this pageChecked 12 November 2026
US FDAFirst approved 20 August 1952Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Import route

Pick the destination country to see the legal import route, who applies and typical timelines, from our import guide for that country.

Import guides are available for 25 countries. Pick one to see its route summary.

BrazilColombiaEgyptEthiopiaGhanaIraqKazakhstanKenyaAll import guides

Alternatives

Other makers and brands of Succinylcholine 200 mg/10 mL injection.

Compare all 2

Other strengths and forms of Succinylcholine

Clinical summary

Succinylcholine is a depolarizing neuromuscular blocker indicated in adults and pediatric patients, among other approved uses. It is available as injection for intramuscular, intravenous and parenteral use. MedsAcross supplies Succinylcholine for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Read about Succinylcholine

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

Data sources

Need Anectine 200 mg/10 mL injection for your hospital or patient?

Send one request with the destination country and quantity. We confirm availability, lead time and the documents your regulator needs.