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Last Updated: March 19, 2026

Details for New Drug Application (NDA): 008453


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NDA 008453 describes ANECTINE, which is a drug marketed by Sandoz and is included in one NDA. It is available from two suppliers. Additional details are available on the ANECTINE profile page.

The generic ingredient in ANECTINE is succinylcholine chloride. There are six drug master file entries for this compound. Thirty suppliers are listed for this compound. Additional details are available on the succinylcholine chloride profile page.
Summary for 008453
Tradename:ANECTINE
Applicant:Sandoz
Ingredient:succinylcholine chloride
Patents:0
Pharmacology for NDA: 008453
Physiological EffectNeuromuscular Depolarizing Blockade
Medical Subject Heading (MeSH) Categories for 008453
Neuromuscular Depolarizing Agents
Suppliers and Packaging for NDA: 008453
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
ANECTINE succinylcholine chloride INJECTABLE;INJECTION 008453 NDA Sandoz Inc 0781-3411 0781-3411-95 10 VIAL, MULTI-DOSE in 1 CARTON (0781-3411-95) / 10 mL in 1 VIAL, MULTI-DOSE (0781-3411-70)
ANECTINE succinylcholine chloride INJECTABLE;INJECTION 008453 NDA Sandoz Inc 0781-9053 0781-9053-95 10 VIAL, MULTI-DOSE in 1 CARTON (0781-9053-95) / 10 mL in 1 VIAL, MULTI-DOSE (0781-9053-70)

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:INJECTABLE;INJECTIONStrength500MG/VIAL
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:No

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrength20MG/ML
Approval Date:Approved Prior to Jan 1, 1982TE:APRLD:Yes

Profile for product number 003

Active Rx/OTC/Discontinued:DISCNDosage:INJECTABLE;INJECTIONStrength50MG/ML
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:No

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Preferred Citation:

Friedman, Yali. "DrugPatentWatch" DrugPatentWatch, thinkBiotech, 2026, www.DrugPatentWatch.com.
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