Oxytocin
Oxytocin 20 USP Units Added to 5% Dextrose/Lactated Ringer's 1,000 mL Bag
Approved
Approval ID
48d3f634-c7f4-48d4-895a-9ef77456cf49
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 Code52533-105
Product Classification
G
Generic Name
Oxytocin
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateDecember 11, 2014
FDA Product Classification
INGREDIENTS (9)
OXYTOCINActive
Quantity: 2 [USP'U] in 100 mL
Code: 1JQS135EYN
Classification: ACTIB
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM CHLORIDEInactive
Quantity: 600 mg in 100 mL
Code: 451W47IQ8X
Classification: IACT
DEXTROSE MONOHYDRATEInactive
Quantity: 5 g in 100 mL
Code: LX22YL083G
Classification: IACT
POTASSIUM CHLORIDEInactive
Quantity: 30 mg in 100 mL
Code: 660YQ98I10
Classification: IACT
SODIUM LACTATEInactive
Quantity: 310 mg in 100 mL
Code: TU7HW0W0QT
Classification: IACT
CALCIUM CHLORIDEInactive
Quantity: 20 mg in 100 mL
Code: M4I0D6VV5M
Classification: IACT
ACETIC ACIDInactive
Code: Q40Q9N063P
Classification: CNTM
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: CNTM