# Midazolam In Sodium Chloride

NDC: 65219-650
Generic name: Midazolam In Sodium Chloride
Labeler / Manufacturer: FRESENIUS KABI USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20250115

FDA application: ANDA218993

## Active ingredients

- MIDAZOLAM HYDROCHLORIDE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65219-650"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65219-650
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c8f51630-e776-4bc6-ba4d-b714e8c3b8f2