Product NDC: | 0143-9689 |
Proprietary Name: | Nicardipine Hydrochloride |
Non Proprietary Name: | Nicardipine Hydrochloride |
Active Ingredient(s): | 25 mg/10mL & nbsp; Nicardipine Hydrochloride |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0143-9689 |
Labeler Name: | West-ward Pharmaceutical Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA022276 |
Marketing Category: | NDA |
Start Marketing Date: | 20120302 |
Package NDC: | 0143-9689-10 |
Package Description: | 10 mL in 1 VIAL (0143-9689-10) |
NDC Code | 0143-9689-10 |
Proprietary Name | Nicardipine Hydrochloride |
Package Description | 10 mL in 1 VIAL (0143-9689-10) |
Product NDC | 0143-9689 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Nicardipine Hydrochloride |
Dosage Form Name | INJECTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20120302 |
Marketing Category Name | NDA |
Labeler Name | West-ward Pharmaceutical Corp |
Substance Name | NICARDIPINE HYDROCHLORIDE |
Strength Number | 25 |
Strength Unit | mg/10mL |
Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |