OXYTOCIN injection, solution

Oxytocin by

Drug Labeling and Warnings

Oxytocin by is a Prescription medication manufactured, distributed, or labeled by Cantrell Drug Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

OXYTOCIN 
oxytocin injection, solution

Product Information
Product Type	HUMAN PRESCRIPTION DRUG	Item Code (Source)	NDC: 52533-233
Route of Administration	INTRAVENOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
OXYTOCIN (UNII: 1JQS135EYN) (OXYTOCIN - UNII:1JQS135EYN)	OXYTOCIN	20 [USP'U]  in 500 mL

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)	3 g  in 500 mL
SODIUM LACTATE (UNII: TU7HW0W0QT)	1.55 g  in 500 mL
POTASSIUM CHLORIDE (UNII: 660YQ98I10)	0.15 g  in 500 mL
CALCIUM CHLORIDE (UNII: M4I0D6VV5M)	0.1 g  in 500 mL
WATER (UNII: 059QF0KO0R)

Other Ingredients
Ingredient Kind	Ingredient Name	Quantity
May contain	ACETIC ACID (UNII: Q40Q9N063P)
May contain	HYDROCHLORIC ACID (UNII: QTT17582CB)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52533-233-30	500 mL in 1 BAG; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		03/18/2016

Labeler - Cantrell Drug Company (035545763)