Drug application

AMITRIPTYLINE HYDROCHLORIDE (AMITRIPTYLINE HYDROCHLORIDE)

Drugs@FDA ANDA 088621 · WATSON LABS

Key facts

Drug name AMITRIPTYLINE HYDROCHLORIDE
Active ingredients AMITRIPTYLINE HYDROCHLORIDE
Application type ANDA
Application number 088621
Company WATSON LABS
Dosage forms TABLET, ORAL
Strength 25MG
Marketing status Discontinued
Reference listed drug No
Latest submission status date Mar 2, 1984

At a glance

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

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