# CUPRIC CHLORIDE

NDC: 80830-2301
Generic name: CUPRIC CHLORIDE
Labeler / Manufacturer: Amneal Pharmaceuticals Private Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20260129

FDA application: ANDA217287

## Active ingredients

- CUPRIC CHLORIDE: .4 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80830-2301"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80830-2301
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c431cc76-f9ba-43c7-8d66-e93c77fa6229