Product NDC: | 52533-050 |
Proprietary Name: | Oxytocin |
Non Proprietary Name: | Oxytocin |
Active Ingredient(s): | 20 [USP'U]/1000mL & nbsp; Oxytocin |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52533-050 |
Labeler Name: | Cantrell Drug Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20111020 |
Package NDC: | 52533-050-24 |
Package Description: | 1000 mL in 1 BAG (52533-050-24) |
NDC Code | 52533-050-24 |
Proprietary Name | Oxytocin |
Package Description | 1000 mL in 1 BAG (52533-050-24) |
Product NDC | 52533-050 |
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 | 20 |
Strength Unit | [USP'U]/1000mL |
Pharmaceutical Classes | Increased Uterine Smooth Muscle Contraction or Tone [PE],Oxytocic [EPC],Oxytocin [Chemical/Ingredient] |