United States · FDA National Drug Code directory

SODIUM CHLORIDE

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
51662-1464_2b39dbc0-2d0b-0a7f-e063-6394a90add31
Product NDC
51662-1464
Form
INJECTION, SOLUTION
Composition / generic term
SODIUM CHLORIDE
Labeler
HF Acquisition Co LLC, DBA HealthFirst
Marketing category
NDA
Marketing start / end (source format)
20191212
Source listing expiry
20261231

Source-listed ingredients

  • SODIUM CHLORIDE — 9 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 20 mL in 1 VIAL, SINGLE-DOSE (51662-1464-1) · 51662-1464-1

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.

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