# Norepinephrine Bitartrate

NDC: 64980-630
Generic name: Norepinephrine Bitartrate
Labeler / Manufacturer: Rising Pharma Holdings, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20241101

FDA application: ANDA218758

## 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:"64980-630"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64980-630
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e6669ed6-9ebc-4b2d-9a8c-5e318fbd18b4