vecuronium bromide
Vecuronium Bromide For Injection
Approved
Approval ID
a14da3ee-a731-4282-be9d-407473517470
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Oct 23, 2018
Manufacturers
FDA
Sun Pharmaceutical Industries, Inc.
DUNS: 146974886
Products 2
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 Code47335-932
Application NumberANDA079001
Product Classification
M
Marketing Category
C73584
G
Generic Name
vecuronium bromide
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateOctober 24, 2018
FDA Product Classification
INGREDIENTS (6)
VECURONIUM BROMIDEActive
Quantity: 1 mg in 1 mL
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
vecuronium bromide
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code47335-931
Application NumberANDA079001
Product Classification
M
Marketing Category
C73584
G
Generic Name
vecuronium bromide
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateOctober 24, 2018
FDA Product Classification
INGREDIENTS (6)
ANHYDROUS CITRIC ACIDInactive
Code: XF417D3PSL
Classification: IACT
VECURONIUM BROMIDEActive
Quantity: 1 mg in 1 mL
Code: 7E4PHP5N1D
Classification: ACTIB
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