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Manufacturing facility

Frontida BioPharm, LLC

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
1100 Orthodox Street, Philadelphia, Pennsylvania (PA) 19124, United States (USA)
Operations here
analysislabelmanufacturepack
FDA identifiers
FEI 2523348 · DUNS 080243260

FDA inspection history

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

  • NAIDrug Quality Assurance2026-04-02
  • VAIDrug Quality Assurance2023-12-07
  • VAIDrug Quality Assurance2019-07-19
  • VAIDrug Quality Assurance2017-03-31
  • OAIDrug Quality Assurance2015-07-17
  • VAIDrug Quality Assurance2014-07-25
  • VAIDrug Quality Assurance2012-01-27
  • VAIDrug Quality Assurance2011-05-20
  • NAIBioresearch Monitoring2009-06-30
  • NAIDrug Quality Assurance2008-12-10

Drugs this plant is listed as making

17 distinct drugs across 56 products name this site in their FDA label.

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.