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
- 0409-5555_bcb3a2dc-1a3f-4ac7-8ea2-426f0771c246
- Product NDC
- 0409-5555
- Form
- INJECTION, SOLUTION
- Composition / generic term
- SODIUM BICARBONATE
- Labeler
- Hospira, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20191021
- Source listing expiry
- 20271231
Source-listed ingredients
- SODIUM BICARBONATE — 42 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 25 VIAL, SINGLE-USE in 1 TRAY (0409-5555-02) / 5 mL in 1 VIAL, SINGLE-USE (0409-5555-12) · 0409-5555-02
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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