Drug application

MYCOPHENOLATE MOFETIL HYDROCHLORIDE (MYCOPHENOLATE MOFETIL HYDROCHLORIDE)

Drugs@FDA ANDA 090311 · BEDFORD LABS

Key facts

Drug name MYCOPHENOLATE MOFETIL HYDROCHLORIDE
Active ingredients MYCOPHENOLATE MOFETIL HYDROCHLORIDE
Application type ANDA
Application number 090311
Company BEDFORD LABS
Dosage forms INJECTABLE, INJECTION
Strength 500MG
Marketing status None (Tentative Approval)
Reference listed drug No
Latest submission status date Sep 30, 2010

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

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