# NICARDIPINE HYDROCHLORIDE

NDC: 35573-458
Generic name: nicardipine hydrochloride
Labeler / Manufacturer: Burel Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20230108

FDA application: ANDA215377

## Active ingredients

- NICARDIPINE HYDROCHLORIDE: 30 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"35573-458"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=35573-458
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cb902af0-b5ad-4680-b2f2-007ef2196efe