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Nicardipine Hydrochloride
Nicardipine Hydrochloride - 42806-501-05 - (Nicardipine Hydrochloride)
Drug Information of Nicardipine Hydrochloride
| Product NDC: | 42806-501 |
| Proprietary Name: | Nicardipine Hydrochloride |
| Non Proprietary Name: | Nicardipine Hydrochloride |
| Active Ingredient(s): | 20 mg/1 & nbsp; Nicardipine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Nicardipine Hydrochloride
| Product NDC: | 42806-501 |
| Labeler Name: | Epic Pharma, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074928 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100505 |
Package Information of Nicardipine Hydrochloride
| Package NDC: | 42806-501-05 |
| Package Description: | 500 CAPSULE in 1 BOTTLE (42806-501-05) |
NDC Information of Nicardipine Hydrochloride
| NDC Code | 42806-501-05 |
| Proprietary Name | Nicardipine Hydrochloride |
| Package Description | 500 CAPSULE in 1 BOTTLE (42806-501-05) |
| Product NDC | 42806-501 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Nicardipine Hydrochloride |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20100505 |
| Marketing Category Name | ANDA |
| Labeler Name | Epic Pharma, LLC |
| Substance Name | NICARDIPINE HYDROCHLORIDE |
| Strength Number | 20 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |
