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Nicardipine Hydrochloride - 42806-501-09 - (Nicardipine Hydrochloride)

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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: 42806-501-09
Package Description: 90 CAPSULE in 1 BOTTLE (42806-501-09)

NDC Information of Nicardipine Hydrochloride

NDC Code 42806-501-09
Proprietary Name Nicardipine Hydrochloride
Package Description 90 CAPSULE in 1 BOTTLE (42806-501-09)
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]

Complete Information of Nicardipine Hydrochloride


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