# Nicardipine Hydrochloride

NDC: 70069-875
Generic name: Nicardipine Hydrochloride
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20260420

FDA application: ANDA220243

## Active ingredients

- NICARDIPINE HYDROCHLORIDE: .1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-875"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-875
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f8b49f59-7a54-425d-9eca-dfa4022a08d1