Overview

Genmab is a biotechnology company headquartered in Valby, Denmark.

API / Drug Master Files

Genmab holds 0 active (1 total) FDA Type II Drug Master File. A Type II DMF is filed with the FDA to support an active ingredient in drug applications; an active filing can be referenced but is not proof of current supply, and inactive filings are historical.

  • HUMAN MONOCLONAL ANTIBODY TO CD4 (ZANOLIMUNAB)Inactive1998-04-15

FDA compliance signals

No FDA recalls, Warning Letters, or Form 483 observations are linked to Genmab in our records. Events are linked by company name and identifier, so this is not proof that none exist; check the FDA's own databases before relying on it.

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