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Manufacturing facility

Supernus Pharmaceuticals Inc

A single plant registered with the FDA to make drugs for the US market. Below is where it is and the drugs whose FDA labels list this site as performing a manufacturing step — so if this plant has a problem, these are the products that could be affected.

Country
United States
Registered address
9715 Key West Ave, Rockville, Maryland (MD) 20850, United States (USA)
Operations here
analysis
FDA identifiers
FEI 3005209462 · DUNS 363066452

FDA inspection history

Outcomes of closed FDA inspections at this site (drug and biologic program areas).

  • NAIDrug Quality Assurance2025-07-31
  • NAIDrug Quality Assurance2019-10-10
  • NAIBioresearch Monitoring2019-07-10
  • VAIBioresearch Monitoring2017-02-03
  • NAIDrug Quality Assurance2015-02-23
  • NAIBioresearch Monitoring2014-06-19

Drugs this plant is listed as making

0 distinct drugs across 0 products name this site in their FDA label.

No drug labels currently list this site.

Sources:the establishment's name, address, and country from FDA's Drug Establishments Current Registration Site (DECRS); the drug-to-facility links from DailyMed SPL drug labels, matched by the facility's DUNS number; inspection outcomes from the FDA Data Dashboard, matched by FEI; shortage status from FDA's drug shortage database. More on how this is built. Educational only.