| Product NDC: | 52533-170 |
| 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) |
| Product NDC: | 52533-170 |
| Labeler Name: | Cantrell Drug Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110701 |
| Package NDC: | 52533-170-32 |
| Package Description: | 500 mL in 1 BAG (52533-170-32) |
| NDC Code | 52533-170-32 |
| Proprietary Name | Oxytocin |
| Package Description | 500 mL in 1 BAG (52533-170-32) |
| Product NDC | 52533-170 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxytocin |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110701 |
| 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] |