Drug application

NORTRIPTYLINE HYDROCHLORIDE (NORTRIPTYLINE HYDROCHLORIDE)

Drugs@FDA ANDA 073556 · DR REDDYS LABS SA

Key facts

Drug name NORTRIPTYLINE HYDROCHLORIDE
Active ingredients NORTRIPTYLINE HYDROCHLORIDE
Application type ANDA
Application number 073556
Company DR REDDYS LABS SA
Dosage forms CAPSULE, ORAL
Strength EQ 75MG BASE
Marketing status Prescription
TE codes AB
Reference listed drug No
Latest submission status date Mar 30, 1992

At a glance

  • 1–9 Submissions
  • 10–99 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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