United States · FDA National Drug Code directory

Sodium Bicarbonate

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
69367-258_43b42880-bab8-4580-8a00-ae13855d44a3
Product NDC
69367-258
Form
TABLET
Composition / generic term
Sodium Bicarbonate
Labeler
Westminster Pharmaceuticals, LLC
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20221010
Source listing expiry
20261231

Source-listed ingredients

  • SODIUM BICARBONATE — 650 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1000 TABLET in 1 BOTTLE (69367-258-10) · 69367-258-10

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

Browse United States records →