Drug application

DV (DIENESTROL)

Drugs@FDA ANDA 083518 · SANOFI AVENTIS US

Key facts

Drug name DV
Active ingredients DIENESTROL
Application type ANDA
Application number 083518
Company SANOFI AVENTIS US
Dosage forms CREAM, VAGINAL
Strength 0.01%
Marketing status Discontinued
Reference listed drug No

At a glance

  • 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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