Oxytocin
Oxytocin 30 USP Units Added to 0.9% Sodium Chloride 500 mL Bag
Approved
Approval ID
06aa4d89-e7a3-417b-bb5e-20ff7058f529
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Dec 11, 2014
Manufacturers
FDA
Cantrell Drug Company
DUNS: 035545763
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Oxytocin
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code52533-056
Product Classification
G
Generic Name
Oxytocin
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateDecember 11, 2014
FDA Product Classification
INGREDIENTS (5)
Sodium ChlorideInactive
Quantity: 4.5 g in 500 mL
Code: 451W47IQ8X
Classification: IACT
WaterInactive
Code: 059QF0KO0R
Classification: IACT
OXYTOCINActive
Quantity: 30 [USP'U] in 500 mL
Code: 1JQS135EYN
Classification: ACTIB
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: CNTM
ACETIC ACIDInactive
Code: Q40Q9N063P
Classification: CNTM