Drug application

LINAGLIPTIN; METFORMIN HYDROCHLORIDE (LINAGLIPTIN;METFORMIN HYDROCHLORIDE)

Drugs@FDA ANDA 214822 · MSN LABORATORIES PRIVATE LTD

Key facts

Drug name LINAGLIPTIN; METFORMIN HYDROCHLORIDE
Active ingredients LINAGLIPTIN;METFORMIN HYDROCHLORIDE
Application type ANDA
Application number 214822
Company MSN LABORATORIES PRIVATE LTD
Dosage forms TABLET, EXTENDED RELEASE, ORAL
Strength 2.5MG/1000
Marketing status None (Tentative Approval)
Reference listed drug No
Latest submission status date Jan 27, 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