Drug application

SODIUM SULFATE, MAGNESIUM SULFATE AND POTASSIUM CHLORIDE (SODIUM SULFATE, MAGNESIUM SULFATE, UNSPECIFIED FORM, POTASSIUM CHLORIDE)

Drugs@FDA ANDA 220421 · HETERO LABS LIMITED, VEMAGAL

Key facts

Drug name SODIUM SULFATE, MAGNESIUM SULFATE AND POTASSIUM CHLORIDE
Active ingredients SODIUM SULFATE, MAGNESIUM SULFATE, UNSPECIFIED FORM, POTASSIUM CHLORIDE
Application type ANDA
Application number 220421
Company HETERO LABS LIMITED, VEMAGAL
Dosage forms TABLET
Strength 1.479G, 0.225G, 0.188G
Marketing status None (Tentative Approval)
Reference listed drug No
Latest submission status date May 1, 2026

At a glance

  • 1–9 Submissions
  • None Label versions
  • None Products
  • None 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

Browse all Drugs@FDA applications