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NICARdipine Hydrochloride
NICARdipine Hydrochloride - 41616-882-44 - (NICARdipine Hydrochloride)
Drug Information of NICARdipine Hydrochloride
| Product NDC: | 41616-882 |
| 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: | 41616-882 |
| Labeler Name: | Sun Pharma Global Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA078405 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20091117 |
Package Information of NICARdipine Hydrochloride
| Package NDC: | 41616-882-44 |
| Package Description: | 10 CARTON in 1 CARTON (41616-882-44) > 1 AMPULE in 1 CARTON (41616-882-40) > 10 mL in 1 AMPULE |
NDC Information of NICARdipine Hydrochloride
| NDC Code | 41616-882-44 |
| Proprietary Name | NICARdipine Hydrochloride |
| Package Description | 10 CARTON in 1 CARTON (41616-882-44) > 1 AMPULE in 1 CARTON (41616-882-40) > 10 mL in 1 AMPULE |
| Product NDC | 41616-882 |
| 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 | NDA |
| Labeler Name | Sun Pharma Global 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] |
