# SODIUM BICARBONATE

NDC: 68462-951
Generic name: SODIUM BICARBONATE
Labeler / Manufacturer: Glenmark Pharmaceuticals Inc., USA
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20250807

FDA application: ANDA219701

## 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:"68462-951"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68462-951
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f38d0dfc-9bcc-4224-a202-885c9ad0beae