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
- 43353-162_36d1abdc-f28b-4c0d-98ea-07718706c695
- Product NDC
- 43353-162
- Form
- TABLET
- Composition / generic term
- SODIUM BICARBONATE
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start / end (source format)
- 20150501
- Source listing expiry
- 20261231
Source-listed ingredients
- SODIUM BICARBONATE — 650 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 60 TABLET in 1 BOTTLE, PLASTIC (43353-162-53) · 43353-162-53
- 90 TABLET in 1 BOTTLE, PLASTIC (43353-162-60) · 43353-162-60
- 120 TABLET in 1 BOTTLE, PLASTIC (43353-162-70) · 43353-162-70
- 180 TABLET in 1 BOTTLE, PLASTIC (43353-162-80) · 43353-162-80
- 200 TABLET in 1 BOTTLE, PLASTIC (43353-162-85) · 43353-162-85
- 360 TABLET in 1 BOTTLE, PLASTIC (43353-162-94) · 43353-162-94
Source and coverage
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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.
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