Suppliers / Titan Pharmaceutical

Titan Pharmaceutical

China 29 employees Updated 9 July 2026

Titan Pharmaceutical is an API manufacturer based in China. It holds 2 valid CEPs across a filed portfolio of 3 molecules. Its GMP standing is certified by ANVISA (Brazil).

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

Registered plants

Site FDA FEI
(GUANGDONG) Heyuan City, China Not on file
HEYUAN, China Not on file

What they file, and where

Molecule Regulators Docs
Cefuroxime SFDA (Saudi Arabia) 1
Cefuroxime Axetil EDQM 1
Cefuroxime Sodium Sterile EDQM 1

Also appears on these molecule pages

Cefuroxime API Cefuroxime Axetil API

Filings and GMP by regulator

Regulator Filings GMP certificates
ANVISA (Brazil) None 1

Questions about Titan Pharmaceutical

Does Titan Pharmaceutical hold a US DMF or a CEP?
Titan Pharmaceutical holds 2 valid CEPs. 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 Titan Pharmaceutical manufacture?
2 registered sites are on record, in China ((guangdong) Heyuan City and Heyuan). Every site is listed on this page with the register it came from.
What does Titan Pharmaceutical make?
3 molecules are on record against Titan Pharmaceutical, including Cefuroxime, Cefuroxime Axetil and Cefuroxime Sodium Sterile. Each links through to that molecule's full manufacturer list.
Which regulators recognise Titan Pharmaceutical's GMP?
Current GMP certificates are on record from ANVISA (Brazil). GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

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.

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Apitoria Pharma shares 2 molecules Orchid Pharma shares 2 molecules Nectar Lifesciences shares 2 molecules Covalent Laboratories shares 2 molecules Zhejiang Dongying Pharmaceutical shares 2 molecules

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
EudraGMDP and national regulators
GMP certificates