# Calcium Gluconate

NDC: 65219-162
Generic name: Calcium Gluconate
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20210617

FDA application: NDA208418

## Active ingredients

- CALCIUM GLUCONATE MONOHYDRATE: 20 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65219-162"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65219-162
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7f5101e0-abf9-4fcf-8986-c799e3333434