# NOREPINEPHRINE BITARTRATE

NDC: 83854-017
Generic name: NOREPINEPHRINE BITARTRATE
Labeler / Manufacturer: Anthea Pharma Private Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION, CONCENTRATE
Routes: INTRAVENOUS
Marketing started: 20251125

FDA application: ANDA219924

## 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:"83854-017"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83854-017
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=52e22892-4fc3-4f53-9f39-0b5c66da3040