Succinylcholine Chloride
Succinylcholine Chloride Injection, USP
Approved
Approval ID
4a63029a-a7c6-43f7-b485-c14ef7a4e92b
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 30, 2023
Manufacturers
FDA
Nexus Pharmaceuticals Inc
DUNS: 620714787
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Succinylcholine Chloride
PRODUCT DETAILS
NDC Product Code14789-104
Application NumberANDA213552
Marketing CategoryC73584
Route of AdministrationINTRAVENOUS, INTRAMUSCULAR
Effective DateMay 30, 2023
Generic NameSuccinylcholine Chloride
INGREDIENTS (6)
Succinylcholine ChlorideActive
Quantity: 20 mg in 1 mL
Code: I9L0DDD30I
Classification: ACTIB
MethylparabenInactive
Quantity: 1.8 mg in 1 mL
Code: A2I8C7HI9T
Classification: IACT
PropylparabenInactive
Quantity: 0.2 mg in 1 mL
Code: Z8IX2SC1OH
Classification: IACT
Sodium ChlorideInactive
Code: 451W47IQ8X
Classification: IACT
Sodium HydroxideInactive
Code: 55X04QC32I
Classification: IACT
Hydrochloric AcidInactive
Code: QTT17582CB
Classification: IACT