Product NDC: | 62778-118 |
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) |
Product NDC: | 62778-118 |
Labeler Name: | Hikma Farmaceutica |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA200219 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090801 |
Package NDC: | 62778-118-03 |
Package Description: | 25 CARTON in 1 CARTON (62778-118-03) > 1 mL in 1 CARTON (62778-118-01) |
NDC Code | 62778-118-03 |
Proprietary Name | Oxytocin |
Package Description | 25 CARTON in 1 CARTON (62778-118-03) > 1 mL in 1 CARTON (62778-118-01) |
Product NDC | 62778-118 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Oxytocin |
Dosage Form Name | INJECTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20090801 |
Marketing Category Name | ANDA |
Labeler Name | Hikma Farmaceutica |
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] |