Product NDC: | 52584-142 |
Proprietary Name: | PHENYLEPHRINE HYDROCHLORIDE |
Non Proprietary Name: | phenylephrine hydrochloride |
Active Ingredient(s): | 10 mg/mL & nbsp; phenylephrine hydrochloride |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52584-142 |
Labeler Name: | General Injectables & Vaccines, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA203826 |
Marketing Category: | NDA |
Start Marketing Date: | 20130402 |
Package NDC: | 52584-142-01 |
Package Description: | 1 VIAL in 1 BAG (52584-142-01) > 1 mL in 1 VIAL |
NDC Code | 52584-142-01 |
Proprietary Name | PHENYLEPHRINE HYDROCHLORIDE |
Package Description | 1 VIAL in 1 BAG (52584-142-01) > 1 mL in 1 VIAL |
Product NDC | 52584-142 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | phenylephrine hydrochloride |
Dosage Form Name | INJECTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20130402 |
Marketing Category Name | NDA |
Labeler Name | General Injectables & Vaccines, Inc |
Substance Name | PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 10 |
Strength Unit | mg/mL |
Pharmaceutical Classes |