DailyMed label

Sodium Chloride

DailyMed label · Nexus Pharmaceuticals LLC · version 4

Key facts

Product Sodium Chloride
Labeler Nexus Pharmaceuticals LLC
Document type HUMAN PRESCRIPTION DRUG LABEL
Active ingredients SODIUM CHLORIDE
Active ingredient UNIIs 451W47IQ8X
Application number 217535
Route INTRAVENOUS, INTRAMUSCULAR, SUBCUTANEOUS
NDC package codes 14789-133-07, 14789-133-05, 14789-134-07, 14789-134-05
Effective date Oct 1, 2024
Set ID 56455921-0c66-4d43-b993-3757b6983041

At a glance

  • 1–9 NDC package codes
  • 1–9 Active ingredients
  • 1–9 Manufacturing establishments listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About DailyMed drug labels

DailyMed publishes the structured product labeling (SPL) that companies submit to the FDA, including package NDCs, ingredients and the establishments that make each product.

Source: U.S. National Library of Medicine (NLM), DailyMed · Source date:

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