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Nicardipine Hydrochloride - 67457-224-10 - (nicardipine hydrochloride)

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Drug Information of Nicardipine Hydrochloride

Product NDC: 67457-224
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): POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Nicardipine Hydrochloride

Product NDC: 67457-224
Labeler Name: Mylan Institutional LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090664
Marketing Category: ANDA
Start Marketing Date: 20111223

Package Information of Nicardipine Hydrochloride

Package NDC: 67457-224-10
Package Description: 10 VIAL in 1 CARTON (67457-224-10) > 10 mL in 1 VIAL (67457-224-00)

NDC Information of Nicardipine Hydrochloride

NDC Code 67457-224-10
Proprietary Name Nicardipine Hydrochloride
Package Description 10 VIAL in 1 CARTON (67457-224-10) > 10 mL in 1 VIAL (67457-224-00)
Product NDC 67457-224
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name nicardipine hydrochloride
Dosage Form Name POWDER, FOR SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20111223
Marketing Category Name ANDA
Labeler Name Mylan Institutional LLC
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]

Complete Information of Nicardipine Hydrochloride


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