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Manufacturing facility

Luoxin Aurovitas Pharma (Chengdu) 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
China
Registered address
No.800, Haifa Road, Chengdu Cross-strait Science and Technology Industrial Development Park, Wenjiang District, Chengdu, Sichuan 611130, China (CHN)
Operations here
analysismanufacture
FDA identifiers
FEI 3019967180 · DUNS 404080894

Drugs this plant is listed as making

2 distinct drugs across 12 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.