Home
>
National Drug Code (NDC)
>
Nicardipine Hydrochloride
Nicardipine Hydrochloride - 0781-3204-95 - (Nicardipine Hydrochloride)
Drug Information of Nicardipine Hydrochloride
| Product NDC: | 0781-3204 |
| Proprietary Name: | Nicardipine Hydrochloride |
| Non Proprietary Name: | Nicardipine Hydrochloride |
| Active Ingredient(s): | 2.5 mg/mL & nbsp; Nicardipine Hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nicardipine Hydrochloride
| Product NDC: | 0781-3204 |
| Labeler Name: | Sandoz Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090125 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091117 |
Package Information of Nicardipine Hydrochloride
| Package NDC: | 0781-3204-95 |
| Package Description: | 10 CARTON in 1 CARTON (0781-3204-95) > 1 VIAL, SINGLE-DOSE in 1 CARTON (0781-3204-70) > 10 mL in 1 VIAL, SINGLE-DOSE |
NDC Information of Nicardipine Hydrochloride
| NDC Code | 0781-3204-95 |
| Proprietary Name | Nicardipine Hydrochloride |
| Package Description | 10 CARTON in 1 CARTON (0781-3204-95) > 1 VIAL, SINGLE-DOSE in 1 CARTON (0781-3204-70) > 10 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0781-3204 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nicardipine Hydrochloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20091117 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc. |
| Substance Name | NICARDIPINE HYDROCHLORIDE |
| Strength Number | 2.5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |
