Home
>
National Drug Code (NDC)
>
Oxytocin
Oxytocin - 62778-119-03 - (Oxytocin)
Drug Information of Oxytocin
| Product NDC: | 62778-119 |
| Proprietary Name: | Oxytocin |
| Non Proprietary Name: | Oxytocin |
| Active Ingredient(s): | 100 [USP'U]/10mL & nbsp; Oxytocin |
| Administration Route(s): | INTRAMUSCULAR; INTRAVASCULAR |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxytocin
| Product NDC: | 62778-119 |
| Labeler Name: | Hikma Farmaceutica |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA200219 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090801 |
Package Information of Oxytocin
| Package NDC: | 62778-119-03 |
| Package Description: | 25 VIAL, MULTI-DOSE in 1 CARTON (62778-119-03) > 10 mL in 1 VIAL, MULTI-DOSE (62778-119-01) |
NDC Information of Oxytocin
| NDC Code | 62778-119-03 |
| Proprietary Name | Oxytocin |
| Package Description | 25 VIAL, MULTI-DOSE in 1 CARTON (62778-119-03) > 10 mL in 1 VIAL, MULTI-DOSE (62778-119-01) |
| Product NDC | 62778-119 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Oxytocin |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVASCULAR |
| Start Marketing Date | 20090801 |
| Marketing Category Name | ANDA |
| Labeler Name | Hikma Farmaceutica |
| Substance Name | OXYTOCIN |
| Strength Number | 100 |
| Strength Unit | [USP'U]/10mL |
| Pharmaceutical Classes | Increased Uterine Smooth Muscle Contraction or Tone [PE],Oxytocic [EPC],Oxytocin [Chemical/Ingredient] |
