# Norepinephrine Bitartrate

NDC: 71288-439
Generic name: Norepinephrine Bitartrate
Labeler / Manufacturer: Meitheal Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION, CONCENTRATE
Routes: INTRAVENOUS
Marketing started: 20241201

FDA application: ANDA040455

## 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:"71288-439"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71288-439
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=53578ac5-b510-4698-a097-f785bfea9fc0