Suppliers / Taizhou Taifa Pharmaceuticals

Taizhou Taifa Pharmaceuticals

China Updated 9 July 2026

Taizhou Taifa Pharmaceuticals is an API manufacturer based in China. It holds 2 active US drug master files and one valid CEP across a filed portfolio of 2 molecules.

2
active US DMFs
1
valid CEPs
1
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Xianju, China Not on file

What they file, and where

Molecule Regulators Docs
Megestrol Acetate EDQM, US FDA 2
Medroxyprogesterone Acetate US FDA 1

Also appears on these molecule pages

Medroxyprogesterone API Megestrol API

Questions about Taizhou Taifa Pharmaceuticals

Does Taizhou Taifa Pharmaceuticals hold a US DMF or a CEP?
Taizhou Taifa Pharmaceuticals holds 2 active US drug master files and 1 valid CEP. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Where does Taizhou Taifa Pharmaceuticals manufacture?
1 registered site is on record, in China (Xianju). Every site is listed on this page with the register it came from.
What does Taizhou Taifa Pharmaceuticals make?
2 molecules are on record against Taizhou Taifa Pharmaceuticals, including Megestrol Acetate and Medroxyprogesterone Acetate. Each links through to that molecule's full manufacturer list.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

Comparing suppliers?

Choose your molecules and target markets. Taizhou Taifa Pharmaceuticals comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Comparable suppliers

Farmabios shares 2 molecules zhejiang xianju pharmaceutical shares 2 molecules Jiangsu Grand Xianle Pharmaceutical shares 2 molecules Zhejiang Xianju Yangguang Bioproducts shares 2 molecules Curia shares 1 molecule

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability