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Oxytocin

Oxytocin 20 USP Units Added to Lactated Ringer's 500 mL Bag

Approved
Approval ID

cf2129df-14c6-45be-89b1-9d8b65d56395

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 Code52533-233
Application NumberN/A
Marketing CategoryN/A
Route of AdministrationINTRAVENOUS
Effective DateMarch 18, 2016
Generic NameOxytocin

INGREDIENTS (8)

SODIUM LACTATEInactive
Quantity: 1.55 g in 500 mL
Code: TU7HW0W0QT
Classification: IACT
OXYTOCINActive
Quantity: 20 [USP'U] in 500 mL
Code: 1JQS135EYN
Classification: ACTIB
SODIUM CHLORIDEInactive
Quantity: 3 g in 500 mL
Code: 451W47IQ8X
Classification: IACT
CALCIUM CHLORIDEInactive
Quantity: 0.1 g in 500 mL
Code: M4I0D6VV5M
Classification: IACT
ACETIC ACIDInactive
Code: Q40Q9N063P
Classification: CNTM
WATERInactive
Code: 059QF0KO0R
Classification: IACT
POTASSIUM CHLORIDEInactive
Quantity: 0.15 g in 500 mL
Code: 660YQ98I10
Classification: IACT
HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: CNTM

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Oxytocin - FDA Drug Approval Details