# NOREPINEPHRINE BITARTRATE

NDC: 47335-615
Generic name: NOREPINEPHRINE BITARTRATE
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION, CONCENTRATE
Routes: INTRAVENOUS
Marketing started: 20210701

FDA application: ANDA211980

## 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:"47335-615"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-615
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4bb42f07-a41e-42f3-92e7-dab665584f84