OXYTOCIN INJECTION, SOLUTION [CANTRELL DRUG COMPANY]

OXYTOCIN INJECTION, SOLUTION [CANTRELL DRUG COMPANY]
PDF | XML

NDC	52533-233-30
Set ID	cf2129df-14c6-45be-89b1-9d8b65d56395
Category	HUMAN PRESCRIPTION DRUG LABEL
Packager	Cantrell Drug Company
Generic Name
Product Class
Product Number
Application Number

View All Sections

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

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

Ingredient Name	Strength
Inactive Ingredients
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)

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

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

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

Labeler - Cantrell Drug Company (035545763)

View All Sections

Related Drugs