# SODIUM BICARBONATE

NDC: 51662-1497
Generic name: SODIUM BICARBONATE
Labeler / Manufacturer: HF Acquisition Co LLC, DBA HealthFirst
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20200218

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:"51662-1497"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51662-1497
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9ee46a5b-d00e-4254-e053-2995a90aeb3a