Oxytocin - 0641-6115-25 - (Oxytocin)

Alphabetical Index


Drug Information of Oxytocin

Product NDC: 0641-6115
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
Coding System: National Drug Codes(NDC)

Labeler Information of Oxytocin

Product NDC: 0641-6115
Labeler Name: West-Ward Pharmaceutical Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA018243
Marketing Category: NDA
Start Marketing Date: 19800429

Package Information of Oxytocin

Package NDC: 0641-6115-25
Package Description: 25 VIAL in 1 CARTON (0641-6115-25) > 10 mL in 1 VIAL (0641-6115-01)

NDC Information of Oxytocin

NDC Code 0641-6115-25
Proprietary Name Oxytocin
Package Description 25 VIAL in 1 CARTON (0641-6115-25) > 10 mL in 1 VIAL (0641-6115-01)
Product NDC 0641-6115
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxytocin
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 19800429
Marketing Category Name NDA
Labeler Name West-Ward Pharmaceutical Corp.
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