Suppliers / Sci Pharmtech

Sci Pharmtech

Taiwan 4119.TW Updated 9 July 2026

Sci Pharmtech is an API manufacturer based in Taiwan. It holds 13 active US drug master files across a filed portfolio of 15 molecules. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 6 June 2025 as VAI.

13
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
5 of 5 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 6 June 2025 VAI US FDA
  • 5 September 2019 NAI US FDA
  • 15 September 2017 VAI US FDA
  • 19 December 2014 NAI US FDA
  • 20 April 2012 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Taiwan, Taiwan 3004065859

What they file, and where

Molecule Regulators Docs
Valproic Acid SFDA (Saudi Arabia), US FDA 3
Sodium Valproate SFDA (Saudi Arabia) 2
Adenine US FDA 1
Allopurinol US FDA 1
Articaine US FDA 1
Atomoxetine US FDA 1
Brinzolamide US FDA 1
Cannabidiol US FDA 1
Clindamycin US FDA 1
Duloxetine US FDA 1
Show all 15 molecules on file
Duloxetine Hydrochlorie SFDA (Saudi Arabia) 1
Hydroxychloroquine US FDA 1
Loxoprofen US FDA 1
Probucol US FDA 1
Propafenone US FDA 1

Also appears on these molecule pages

Allopurinol API Articaine API Atomoxetine API Brinzolamide API Cannabidiol API Clindamycin API Hydroxychloroquine API Loxoprofen API Propafenone API Sodium Valproate API Valproic Acid API Duloxetine API

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA None 1

Questions about Sci Pharmtech

Does Sci Pharmtech hold a US DMF or a CEP?
Sci Pharmtech holds 13 active US drug master files. 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.
Is Sci Pharmtech FDA-registered?
One site operated by Sci Pharmtech carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Sci Pharmtech's last inspection go?
The most recent inspection on record closed on 6 June 2025 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 5 inspections are on file.
Where does Sci Pharmtech manufacture?
1 registered site is on record, in Taiwan (Taiwan). Every site is listed on this page with the register it came from.
What does Sci Pharmtech make?
15 molecules are on record against Sci Pharmtech, including Valproic Acid, Sodium Valproate, Adenine and Allopurinol. Each links through to that molecule's full manufacturer list.
Which regulators recognise Sci Pharmtech's GMP?
Current GMP certificates are on record from US FDA. 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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Open risk flags

  • 1 active litigation matter is on record.
  • The most recent inspection outcome was VAI, on 6 June 2025.

Comparable suppliers

Zydus Lifesciences shares 4 molecules Harman Finochem shares 3 molecules Assurgen Pharma shares 3 molecules Apitoria Pharma shares 2 molecules Hetero 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