Oxytocin - 63323-012-12 - (OXYTOCIN)

Alphabetical Index


Drug Information of Oxytocin

Product NDC: 63323-012
Proprietary Name: Oxytocin
Non Proprietary Name: OXYTOCIN
Active Ingredient(s): 10    [USP'U]/mL & nbsp;   OXYTOCIN
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Oxytocin

Product NDC: 63323-012
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018248
Marketing Category: NDA
Start Marketing Date: 20000810

Package Information of Oxytocin

Package NDC: 63323-012-12
Package Description: 25 VIAL in 1 TRAY (63323-012-12) > 1 mL in 1 VIAL

NDC Information of Oxytocin

NDC Code 63323-012-12
Proprietary Name Oxytocin
Package Description 25 VIAL in 1 TRAY (63323-012-12) > 1 mL in 1 VIAL
Product NDC 63323-012
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name OXYTOCIN
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20000810
Marketing Category Name NDA
Labeler Name APP Pharmaceuticals, LLC
Substance Name OXYTOCIN
Strength Number 10
Strength Unit [USP'U]/mL
Pharmaceutical Classes Increased Uterine Smooth Muscle Contraction or Tone [PE],Oxytocic [EPC],Oxytocin [Chemical/Ingredient]

Complete Information of Oxytocin


General Information