SUCCINYLCHOLINE CHLORIDE
Succinylcholine Chloride Injection, USP 200 mg/10 mL (20 mg/mL) Rx only
Approved
Approval ID
896a4238-667d-45b0-e053-2a95a90a60dd
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
May 15, 2023
Manufacturers
FDA
Medical Purchasing Solutions, LLC
DUNS: 601458529
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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code71872-7166
Application NumberANDA211432
Product Classification
M
Marketing Category
C73584
G
Generic Name
SUCCINYLCHOLINE CHLORIDE
Product Specifications
Route of AdministrationINTRAMUSCULAR, INTRAVENOUS
Effective DateMay 15, 2023
FDA Product Classification
INGREDIENTS (7)
PROPYLPARABENInactive
Quantity: 0.2 mg in 1 mL
Code: Z8IX2SC1OH
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM CHLORIDEInactive
Code: 451W47IQ8X
Classification: IACT
METHYLPARABENInactive
Quantity: 1.8 mg in 1 mL
Code: A2I8C7HI9T
Classification: IACT
HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: IACT
SUCCINYLCHOLINE CHLORIDEActive
Quantity: 20 mg in 1 mL
Code: I9L0DDD30I
Classification: ACTIB