# Ascorbic Acid

NDC: 65219-027
Generic name: Ascorbic Acid
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20251208

FDA application: ANDA217131

## Active ingredients

- ASCORBIC ACID: 500 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65219-027"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65219-027
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1606e29f-0e80-4069-b688-daab9cbff20a