# Nicardipine Hydrochloride

NDC: 69452-437
Generic name: Nicardipine Hydrochloride
Labeler / Manufacturer: Bionpharma Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20241104

FDA application: ANDA217555

## 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:"69452-437"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69452-437
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7bed5d8c-30c2-4598-acf3-2edba825a56d