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

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA None 1

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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.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates