Drug application

BAMATE (MEPROBAMATE)

Drugs@FDA ANDA 080380 · ALRA

Key facts

Drug name BAMATE
Active ingredients MEPROBAMATE
Application type ANDA
Application number 080380
Company ALRA
Dosage forms TABLET, ORAL
Strength 200MG
Marketing status Discontinued
Reference listed drug No
Latest submission status date Jul 29, 1971

At a glance

  • 1–9 Submissions
  • 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

Browse all Drugs@FDA applications