Product NDC: | 42806-502 |
Proprietary Name: | Nicardipine Hydrochloride |
Non Proprietary Name: | Nicardipine Hydrochloride |
Active Ingredient(s): | 30 mg/1 & nbsp; Nicardipine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 42806-502 |
Labeler Name: | Epic Pharma, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA074928 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100505 |
Package NDC: | 42806-502-10 |
Package Description: | 1000 CAPSULE in 1 BOTTLE (42806-502-10) |
NDC Code | 42806-502-10 |
Proprietary Name | Nicardipine Hydrochloride |
Package Description | 1000 CAPSULE in 1 BOTTLE (42806-502-10) |
Product NDC | 42806-502 |
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 | 30 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |