Drug application

MESALAMINE (MESALAMINE)

Drugs@FDA ANDA 211858 · SUN PHARM

Key facts

Drug name MESALAMINE
Active ingredients MESALAMINE
Application type ANDA
Application number 211858
Company SUN PHARM
Dosage forms TABLET, DELAYED RELEASE, ORAL
Strength 1.2GM
Marketing status Prescription
TE codes AB
Reference listed drug No
Latest submission status date Jan 25, 2019

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

Browse all Drugs@FDA applications