MedPath

Oxytocin

Oxytocin 30 USP Units Added to Lactated Ringer's 500 mL Bag

Approved
Approval ID

736b2590-79e8-4bd0-ab54-84ff7e29a030

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Dec 24, 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 Code52533-055
Product Classification
G
Generic Name
Oxytocin
Product Specifications
Route of AdministrationINTRAVENOUS
Effective DateDecember 24, 2014
FDA Product Classification

INGREDIENTS (8)

CALCIUM CHLORIDEInactive
Quantity: 0.1 g in 500 mL
Code: M4I0D6VV5M
Classification: IACT
HYDROCHLORIC ACIDInactive
Code: QTT17582CB
Classification: CNTM
SODIUM LACTATEInactive
Quantity: 1.55 g in 500 mL
Code: TU7HW0W0QT
Classification: IACT
OXYTOCINActive
Quantity: 30 [USP'U] in 500 mL
Code: 1JQS135EYN
Classification: ACTIB
SODIUM CHLORIDEInactive
Quantity: 3 g in 500 mL
Code: 451W47IQ8X
Classification: IACT
POTASSIUM CHLORIDEInactive
Quantity: 0.15 g in 500 mL
Code: 660YQ98I10
Classification: IACT
WATERInactive
Code: 059QF0KO0R
Classification: IACT
ACETIC ACIDInactive
Code: Q40Q9N063P
Classification: CNTM

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.

Oxytocin - FDA Drug Approval Details