Drug application

METHYLDOPA (METHYLDOPA)

Drugs@FDA ANDA 070331 · PARKE DAVIS

Key facts

Drug name METHYLDOPA
Active ingredients METHYLDOPA
Application type ANDA
Application number 070331
Company PARKE DAVIS
Dosage forms TABLET, ORAL
Strength 125MG
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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