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
57237-361_7269ab59-c9e8-4e4f-b3c9-72d40f7abbb8
Product NDC
57237-361
Form
TABLET
Composition / generic term
Sodium Chloride
Labeler
Rising Pharma Holdings, Inc.
Marketing category
OTC MONOGRAPH DRUG
Marketing start / end (source format)
20251106
Source listing expiry
20261231

Source-listed ingredients

  • SODIUM CHLORIDE — 1000 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 TABLET in 1 BOTTLE (57237-361-01) · 57237-361-01

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 →