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Nicardipine Hydrochloride - 0143-9689-10 - (Nicardipine Hydrochloride)

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Drug Information of Nicardipine Hydrochloride

Product NDC: 0143-9689
Proprietary Name: Nicardipine Hydrochloride
Non Proprietary Name: Nicardipine Hydrochloride
Active Ingredient(s): 25    mg/10mL & nbsp;   Nicardipine Hydrochloride
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Nicardipine Hydrochloride

Product NDC: 0143-9689
Labeler Name: West-ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022276
Marketing Category: NDA
Start Marketing Date: 20120302

Package Information of Nicardipine Hydrochloride

Package NDC: 0143-9689-10
Package Description: 10 mL in 1 VIAL (0143-9689-10)

NDC Information of Nicardipine Hydrochloride

NDC Code 0143-9689-10
Proprietary Name Nicardipine Hydrochloride
Package Description 10 mL in 1 VIAL (0143-9689-10)
Product NDC 0143-9689
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nicardipine Hydrochloride
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20120302
Marketing Category Name NDA
Labeler Name West-ward Pharmaceutical Corp
Substance Name NICARDIPINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/10mL
Pharmaceutical Classes Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient]

Complete Information of Nicardipine Hydrochloride


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