Oxytocin
Oxytocin 30 USP Units Added to 5% Dextrose/0.45% Sodium Chloride 1,000 mL Bag
Approved
Approval ID
c7a56694-0314-4b2d-965e-c665e7453e5b
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Mar 18, 2016
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 Code52533-234
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationINTRAVENOUS
Effective DateMarch 18, 2016
Generic NameOxytocin
INGREDIENTS (6)
OXYTOCINActive
Quantity: 30 [USP'U] in 1000 mL
Code: 1JQS135EYN
Classification: ACTIB
DEXTROSE MONOHYDRATEInactive
Quantity: 50 g in 1000 mL
Code: LX22YL083G
Classification: IACT
SODIUM CHLORIDEInactive
Quantity: 4.5 g in 1000 mL
Code: 451W47IQ8X
Classification: IACT
ACETIC ACIDInactive
Code: Q40Q9N063P
Classification: CNTM
SODIUM HYDROXIDEInactive
Code: 55X04QC32I
Classification: CNTM
WATERInactive
Code: 059QF0KO0R
Classification: IACT