Drug application

POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)

Drugs@FDA ANDA 209688 · TWI PHARMS

Key facts

Drug name POTASSIUM CHLORIDE
Active ingredients POTASSIUM CHLORIDE
Application type ANDA
Application number 209688
Company TWI PHARMS
Dosage forms TABLET, EXTENDED RELEASE, ORAL
Strength 10MEQ
Marketing status Prescription
TE codes AB3
Reference listed drug No
Latest submission status date Jan 12, 2018

At a glance

  • 1–9 Submissions
  • 1–9 Supplements
  • None Label versions
  • 1–9 Products
  • 1–9 Therapeutic equivalents

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

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