Drug application

POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)

Drugs@FDA NDA 208019 · GENUS

Key facts

Drug name POTASSIUM CHLORIDE
Active ingredients POTASSIUM CHLORIDE
Application type NDA
Application number 208019
Company GENUS
Dosage forms FOR SOLUTION, ORAL
Strength 20MEQ
Marketing status Prescription
TE codes AA
Reference listed drug Yes
Latest submission class Type 7 - Drug Already Marketed without Approved NDA
Latest submission status date Aug 19, 2015

At a glance

  • 1–9 Submissions
  • 1–9 Supplements
  • 1–9 Label versions
  • 1–9 Products
  • 10–99 Therapeutic equivalents
  • Yes FDA letters on file
  • Yes FDA reviews on file

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

About Drugs@FDA applications

Drugs@FDA covers FDA-approved brand-name and generic drugs and therapeutic biologics, with their applications (NDA, ANDA or BLA), products, submissions and labels.

Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date:

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