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Manufacturing facility

Lonza Tampa 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
5709 JOHNS RD SUITE 1209, TAMPA, Florida (FL) 33634, United States (USA)
Operations here
manufacture
FDA identifiers
FEI 3001549109 · DUNS 080939373

FDA inspection history

Outcomes of closed FDA inspections at this site, every FDA program area; the official-action banner above considers Drug Quality Assurance inspections only.

  • VAIDrug Quality Assurance2025-08-22
  • VAIDrug Quality Assurance2023-09-29
  • VAIDrug Quality Assurance2021-10-01
  • VAIDrug Quality Assurance2018-07-20
  • VAIDrug Quality Assurance2017-07-14
  • VAIDrug Quality Assurance2008-12-10

Drugs this plant is listed as making

1 distinct drugs across 1 products name this site for a manufacturing step (any MANUFACTURE-type role, API included). Counts are per distinct generic name (case-insensitive).

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.