# Norepinephrine Bitartrate

NDC: 65219-140
Generic name: NOREPINEPHRINE BITARTRATE
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: INTRAVENOUS
Marketing started: 20210301

FDA application: ANDA211382

## Active ingredients

- NOREPINEPHRINE BITARTRATE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"65219-140"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65219-140
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dfed53ef-2060-44b8-a62e-9f8ee10a05a5