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