DailyMed label

Potassium Chloride

DailyMed label · Amneal Pharmaceuticals NY LLC · version 12

Key facts

Product Potassium Chloride
Labeler Amneal Pharmaceuticals NY LLC
Document type HUMAN PRESCRIPTION DRUG LABEL
Active ingredients POTASSIUM CHLORIDE
Active ingredient UNIIs 660YQ98I10
Application number 210041
Route ORAL
NDC package codes 69238-1459-2, 69238-1459-3, 69238-1459-4, 69238-1458-2, 69238-1458-3, 69238-1458-4
Effective date Jul 1, 2026
Set ID 590dd25c-c4cb-489a-a09b-eccbf1d37c1f

At a glance

  • 1–9 NDC package codes
  • 1–9 Active ingredients
  • None Manufacturing establishments listed

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

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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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