# Sodium Bicarbonate

NDC: 72603-209
Generic name: SODIUM BICARBONATE
Labeler / Manufacturer: NORTHSTAR RX LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20240219
Marketing ended: 20260630
FDA application: ANDA216364

## Active ingredients

- SODIUM BICARBONATE: 84 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72603-209"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72603-209
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=068db1fe-0346-48f1-8d2f-8488d7331106