# sodium bicarbonate

NDC: 0338-0822
Generic name: sodium bicarbonate
Labeler / Manufacturer: Baxter Healthcare Corporation
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20260814

FDA application: NDA218524

## Active ingredients

- SODIUM BICARBONATE: 12.6 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0338-0822"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0338-0822
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b50c858a-00c8-4cb2-ad73-8797f19e656d