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
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code52533-234
Product Classification
G
Generic Name
Oxytocin
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateMarch 18, 2016
FDA Product Classification
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