Yuki Gosei Kogyo Co., Ltd.
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
- Japan
- Registered address
- OCHIAI788, JOBANNISHIGOMACHI, IWAKI, FUKUSHIMA 972-8316, Japan (JPN)
- Operations here
- api manufacture
- FDA identifiers
- FEI 3002808534 · DUNS 706298080
FDA inspection history
Outcomes of closed FDA inspections at this site (drug and biologic program areas).
- VAIDrug Quality Assurance2026-02-06
- VAIDrug Quality Assurance2021-07-28
- OAIDrug Quality Assurance2017-11-17
- VAIDrug Quality Assurance2016-09-02
- NAIDrug Quality Assurance2014-03-07
- VAIDrug Quality Assurance2012-06-22
- OAIDrug Quality Assurance2010-07-21
Drugs this plant is listed as making
2 distinct drugs across 3 products name this site in their FDA label.
- isoniazidCMP Pharma, Inc.
- trifluridine and tipiracilTaiho Pharmaceutical Co., Ltd.
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.