VECURONIUM BROMIDE
Vecuronium Bromide for Injection Rx only
Approved
Approval ID
86d81719-534c-4e50-ae39-d8b20e50dfad
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 6, 2023
Manufacturers
FDA
Eugia US LLC
DUNS: 968961354
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
VECURONIUM BROMIDE
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code55150-235
Application NumberANDA206670
Product Classification
M
Marketing Category
C73584
G
Generic Name
VECURONIUM BROMIDE
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateAugust 29, 2023
FDA Product Classification
INGREDIENTS (6)
VECURONIUM BROMIDEActive
Quantity: 10 mg in 1 1
Code: 7E4PHP5N1D
Classification: ACTIB
ANHYDROUS CITRIC ACIDInactive
Code: XF417D3PSL
Classification: IACT
SODIUM PHOSPHATE, DIBASIC, ANHYDROUSInactive
Code: 22ADO53M6F
Classification: IACT
MANNITOLInactive
Code: 3OWL53L36A
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: IACT
PHOSPHORIC ACIDInactive
Code: E4GA8884NN
Classification: IACT