# Nicardipine Hydrochloride

NDC: 0517-0735
Generic name: nicardipine hydrochloride
Labeler / Manufacturer: American Regent, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20200508

FDA application: ANDA090534

## Active ingredients

- NICARDIPINE HYDROCHLORIDE: 2.5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0517-0735"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0517-0735
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=76fcb7e0-9034-4fcd-be14-ce7e9ccaee2a