# Sodium Bicarbonate

NDC: 51754-5012
Generic name: SODIUM BICARBONATE
Labeler / Manufacturer: Exela Pharma Sciences, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20180927

FDA application: ANDA211091

## Active ingredients

- SODIUM BICARBONATE: 42 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51754-5012"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51754-5012
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e9698a4f-1a95-4f28-a945-e8009d1d6dd4