Product NDC: | 55154-5128 |
Proprietary Name: | Phenylephrine Hydrochloride |
Non Proprietary Name: | Phenylephrine Hydrochloride |
Active Ingredient(s): | 10 mg/mL & nbsp; Phenylephrine Hydrochloride |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-5128 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA203826 |
Marketing Category: | NDA |
Start Marketing Date: | 20121220 |
Package NDC: | 55154-5128-8 |
Package Description: | 1 VIAL in 1 BAG (55154-5128-8) > 1 mL in 1 VIAL |
NDC Code | 55154-5128-8 |
Proprietary Name | Phenylephrine Hydrochloride |
Package Description | 1 VIAL in 1 BAG (55154-5128-8) > 1 mL in 1 VIAL |
Product NDC | 55154-5128 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Phenylephrine Hydrochloride |
Dosage Form Name | INJECTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
Start Marketing Date | 20121220 |
Marketing Category Name | NDA |
Labeler Name | Cardinal Health |
Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes |