# NICARDIPINE HYDROCHLORIDE

NDC: 82432-103
Generic name: Nicardipine Hydrochloride
Labeler / Manufacturer: Chengdu Shuode Pharmaceutical Co., Ltd
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20240911

FDA application: ANDA217548

## Active ingredients

- NICARDIPINE HYDROCHLORIDE: 25 mg/10mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82432-103"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82432-103
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=433dbca3-0a86-44c2-835d-1051c1c93878