Oxytocin
Oxytocin 10 USP Units Added to 0.9% Sodium Chloride 1,000 mL Bag
Approved
Approval ID
dbba90dd-e29c-41fc-b2e9-8c1af162586b
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
NDC Product Code52533-048
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationINTRAVENOUS
Effective DateDecember 11, 2014
Generic NameOxytocin
INGREDIENTS (5)
OXYTOCINActive
Quantity: 10 [USP'U] in 1000 mL
Code: 1JQS135EYN
Classification: ACTIB
SODIUM CHLORIDEInactive
Quantity: 9 g in 1000 mL
Code: 451W47IQ8X
Classification: IACT
ACETIC ACIDInactive
Code: Q40Q9N063P
Classification: CNTM
WATERInactive
Code: 059QF0KO0R
Classification: IACT
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: CNTM