# Sodium Bicarbonate

NDC: 81665-200
Generic name: SODIUM BICARBONATE
Labeler / Manufacturer: OMNIVIUM PHARMACEUTICALS LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20230616

FDA application: ANDA216364

## Active ingredients

- SODIUM BICARBONATE: 84 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"81665-200"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=81665-200
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=aea54f8d-1cdd-4a5c-a2f7-7317ae4c8fbc