Drug application

DIETHYLPROPION HYDROCHLORIDE (DIETHYLPROPION HYDROCHLORIDE)

Drugs@FDA ANDA 091680 · LANNETT CO INC

Key facts

Drug name DIETHYLPROPION HYDROCHLORIDE
Active ingredients DIETHYLPROPION HYDROCHLORIDE
Application type ANDA
Application number 091680
Company LANNETT CO INC
Dosage forms TABLET, EXTENDED RELEASE, ORAL
Strength 75MG
Marketing status Prescription
TE codes AB
Reference listed drug No
Latest submission class Not Applicable
Latest submission status date Oct 24, 2011

At a glance

  • 1–9 Submissions
  • 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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