# Norepinephrine Bitartrate

NDC: 51991-983
Generic name: Norepinephrine Bitartrate
Labeler / Manufacturer: Breckenridge Pharmaceutical, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION, CONCENTRATE
Routes: INTRAVENOUS
Marketing started: 20210701

FDA application: ANDA214455

## 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:"51991-983"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51991-983
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=109aa5e6-4e42-4131-97b0-f24d3a4cb4e8