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Nicardipine Hydrochloride - 64679-631-02 - (Nicardipine Hydrochloride)

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Drug Information of Nicardipine Hydrochloride

Product NDC: 64679-631
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): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Nicardipine Hydrochloride

Product NDC: 64679-631
Labeler Name: Wockhardt USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090671
Marketing Category: ANDA
Start Marketing Date: 20091109

Package Information of Nicardipine Hydrochloride

Package NDC: 64679-631-02
Package Description: 10 CARTON in 1 CARTON (64679-631-02) > 1 VIAL, SINGLE-DOSE in 1 CARTON (64679-631-01) > 10 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Nicardipine Hydrochloride

NDC Code 64679-631-02
Proprietary Name Nicardipine Hydrochloride
Package Description 10 CARTON in 1 CARTON (64679-631-02) > 1 VIAL, SINGLE-DOSE in 1 CARTON (64679-631-01) > 10 mL in 1 VIAL, SINGLE-DOSE
Product NDC 64679-631
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Nicardipine Hydrochloride
Dosage Form Name INJECTION
Route Name INTRAVENOUS
Start Marketing Date 20091109
Marketing Category Name ANDA
Labeler Name Wockhardt USA 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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