Product NDC: | 55154-9554 |
Proprietary Name: | Hydralazine Hydrochloride |
Non Proprietary Name: | HYDRALAZINE HYDROCHLORIDE |
Active Ingredient(s): | 20 mg/mL & nbsp; HYDRALAZINE HYDROCHLORIDE |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-9554 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040388 |
Marketing Category: | ANDA |
Start Marketing Date: | 20110131 |
Package NDC: | 55154-9554-5 |
Package Description: | 5 VIAL, SINGLE-DOSE in 1 BAG (55154-9554-5) > 1 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 55154-9554-5 |
Proprietary Name | Hydralazine Hydrochloride |
Package Description | 5 VIAL, SINGLE-DOSE in 1 BAG (55154-9554-5) > 1 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 55154-9554 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | HYDRALAZINE HYDROCHLORIDE |
Dosage Form Name | INJECTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS |
Start Marketing Date | 20110131 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | HYDRALAZINE HYDROCHLORIDE |
Strength Number | 20 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC] |