Drug application

TRICLOS (TRICLOFOS SODIUM)

Drugs@FDA NDA 016809 · SANOFI AVENTIS US

Key facts

Drug name TRICLOS
Active ingredients TRICLOFOS SODIUM
Application type NDA
Application number 016809
Company SANOFI AVENTIS US
Dosage forms TABLET, ORAL
Strength 750MG
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.

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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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