# Nicardipine Hydrochloride

NDC: 72819-149
Generic name: nicardipine hydrochloride
Labeler / Manufacturer: Archis Pharma LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20241207

FDA application: ANDA090664

## 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:"72819-149"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72819-149
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d0070638-bea5-413a-8658-4c752c6104f5