Pfizer 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
- 875 Chesterfield Parkway W, Chesterfield, Missouri (MO) 63017-0774, United States (USA)
- Operations here
- analysisapi manufacture
- FDA identifiers
- FEI 1940118 · DUNS 004954111
FDA inspection history
Outcomes of closed FDA inspections at this site (drug and biologic program areas).
- NAIDrug Quality Assurance2019-08-20
- VAIDrug Quality Assurance2016-02-16
- NAIDrug Quality Assurance2014-05-21
- NAIDrug Quality Assurance2012-02-29
Drugs this plant is listed as making
4 distinct drugs across 14 products name this site in their FDA label.
- Amlodipine and AtorvastatinPrasco Laboratories
- gemfibrozilParke-Davis Div of Pfizer Inc
- pegfilgrastim-apgfPfizer Laboratories Div Pfizer Inc
- PhenytoinPrasco Laboratories
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.