Oxytocin: Package Insert and Label Information

OXYTOCIN — oxytocin injection, solution
Cantrell Drug Company

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Preparation Label
(click image for full-size original)

OXYTOCIN
oxytocin injection, solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:52533-048
Route of Administration INTRAVENOUS DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
OXYTOCIN (OXYTOCIN) OXYTOCIN 10 [USP’U] in 1000 mL
Inactive Ingredients
Ingredient Name Strength
SODIUM CHLORIDE 9 g in 1000 mL
WATER
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:52533-048-24 1000 mL in 1 BAG None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
unapproved drug other 07/30/2012
Labeler — Cantrell Drug Company (035545763)

Revised: 12/2014 Cantrell Drug Company

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