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FDA Drug Approval, N019734, CARDENE IN 5.0% DEXTROSE IN PLASTIC CONTAINER
FDA Drug Approval, N019734, CARDENE IN 5.0% DEXTROSE IN PLASTIC CONTAINER
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NDA: 019734
Company: CHIESI
Drug Name: CARDENE IN 5.0% DEXTROSE IN PLASTIC CONTAINER
Active Ingredients: NICARDIPINE HYDROCHLORIDE
Strength: 40MG/200ML (0.2MG/ML)
Dosage Form/Route: INJECTABLE;INTRAVENOUS
Action Date: 01/30/1992
Marketing Status: Discontinued
Submission Classification: Type 3 - New Dosage Form
Company: CHIESI
Drug Name: CARDENE IN 5.0% DEXTROSE IN PLASTIC CONTAINER
Active Ingredients: NICARDIPINE HYDROCHLORIDE
Strength: 40MG/200ML (0.2MG/ML)
Dosage Form/Route: INJECTABLE;INTRAVENOUS
Action Date: 01/30/1992
Marketing Status: Discontinued
Submission Classification: Type 3 - New Dosage Form
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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