# Nicardipine Hydrochloride

NDC: 68462-121
Generic name: Nicardipine Hydrochloride
Labeler / Manufacturer: Glenmark Pharmaceuticals Inc., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20221216

FDA application: ANDA216357

## 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:"68462-121"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-121
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3955d43d-a87f-4d2c-b90e-3ecf0d6aa148