Oxytocin - 42023-141-25 - (oxytocin)

Alphabetical Index


Drug Information of Oxytocin

Product NDC: 42023-141
Proprietary Name: Oxytocin
Non Proprietary Name: oxytocin
Active Ingredient(s): 10    [iU]/mL & nbsp;   oxytocin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Oxytocin

Product NDC: 42023-141
Labeler Name: JHP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018261
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20120601

Package Information of Oxytocin

Package NDC: 42023-141-25
Package Description: 25 VIAL in 1 CARTON (42023-141-25) > 10 mL in 1 VIAL

NDC Information of Oxytocin

NDC Code 42023-141-25
Proprietary Name Oxytocin
Package Description 25 VIAL in 1 CARTON (42023-141-25) > 10 mL in 1 VIAL
Product NDC 42023-141
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxytocin
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20120601
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name JHP Pharmaceuticals, LLC
Substance Name OXYTOCIN
Strength Number 10
Strength Unit [iU]/mL
Pharmaceutical Classes Increased Uterine Smooth Muscle Contraction or Tone [PE],Oxytocic [EPC],Oxytocin [Chemical/Ingredient]

Complete Information of Oxytocin


General Information