# Sodium Bicarbonate

NDC: 0409-5555
Generic name: SODIUM BICARBONATE
Labeler / Manufacturer: Hospira, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20191021

FDA application: ANDA202981

## Active ingredients

- SODIUM BICARBONATE: 42 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0409-5555"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0409-5555
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ea9f4498-0d43-4043-8dd1-f22537841c21