Drug application

MEPROSPAN (MEPROBAMATE)

Drugs@FDA NDA 011284 · MEDPOINTE PHARM HLC

Key facts

Drug name MEPROSPAN
Active ingredients MEPROBAMATE
Application type NDA
Application number 011284
Company MEDPOINTE PHARM HLC
Dosage forms CAPSULE, EXTENDED RELEASE, ORAL
Strength 200MG
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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