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
51662-1255_100d6df7-3403-6068-e063-6294a90a74f3
Product NDC
51662-1255
Form
INJECTION, SOLUTION
Composition / generic term
SODIUM BICARBONATE
Labeler
HF Acquisition Co LLC, DBA HealthFirst
Marketing category
UNAPPROVED DRUG OTHER
Marketing start / end (source format)
20180917
Source listing expiry
20261231

Source-listed ingredients

  • SODIUM BICARBONATE — 84 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 SYRINGE in 1 CARTON (51662-1255-1) / 50 mL in 1 SYRINGE · 51662-1255-1

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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