Oxytocin - 52533-055-29 - (Oxytocin)

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Drug Information of Oxytocin

Product NDC: 52533-055
Proprietary Name: Oxytocin
Non Proprietary Name: Oxytocin
Active Ingredient(s): 30    [USP'U]/500mL & nbsp;   Oxytocin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Oxytocin

Product NDC: 52533-055
Labeler Name: Cantrell Drug Company
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20111020

Package Information of Oxytocin

Package NDC: 52533-055-29
Package Description: 500 mL in 1 BAG (52533-055-29)

NDC Information of Oxytocin

NDC Code 52533-055-29
Proprietary Name Oxytocin
Package Description 500 mL in 1 BAG (52533-055-29)
Product NDC 52533-055
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxytocin
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20111020
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Cantrell Drug Company
Substance Name OXYTOCIN
Strength Number 30
Strength Unit [USP'U]/500mL
Pharmaceutical Classes Increased Uterine Smooth Muscle Contraction or Tone [PE],Oxytocic [EPC],Oxytocin [Chemical/Ingredient]

Complete Information of Oxytocin


General Information