Drug application

METHYLDOPA AND HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDE, METHYLDOPA)

Drugs@FDA ANDA 071460 · IVAX SUB TEVA PHARMS

Key facts

Drug name METHYLDOPA AND HYDROCHLOROTHIAZIDE
Active ingredients HYDROCHLOROTHIAZIDE, METHYLDOPA
Application type ANDA
Application number 071460
Company IVAX SUB TEVA PHARMS
Dosage forms TABLET, ORAL
Strength 30MG;500MG
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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