Suppliers / DDP Specialty Electronic Materials US 9

DDP Specialty Electronic Materials US 9

United States Updated 9 July 2026

DDP Specialty Electronic Materials US 9 is an API manufacturer based in United States. It appears in 2 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 16 April 2025 as NAI.

0
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
2
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
6 of 6 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 16 April 2025 NAI US FDA
  • 7 November 2018 VAI US FDA
  • 24 January 2014 VAI US FDA
  • 18 May 2012 VAI US FDA
  • 29 June 2011 VAI US FDA
  • 8 July 2009 VAI US FDA

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

Registered plants

Site FDA FEI
Hemlock, United States 1816403

What they file, and where

Molecule Regulators Docs
Simethicone SFDA (Saudi Arabia) 3

Also appears on these molecule pages

Simethicone API

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 2 None
US FDA None 1

Questions about DDP Specialty Electronic Materials US 9

Does DDP Specialty Electronic Materials US 9 hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for DDP Specialty Electronic Materials US 9. It does have 2 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Is DDP Specialty Electronic Materials US 9 FDA-registered?
One site operated by DDP Specialty Electronic Materials US 9 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 DDP Specialty Electronic Materials US 9's last inspection go?
The most recent inspection on record closed on 16 April 2025 as NAI (No Action Indicated: nothing objectionable was found). 6 inspections are on file.
Where does DDP Specialty Electronic Materials US 9 manufacture?
1 registered site is on record, in United States (Hemlock). Every site is listed on this page with the register it came from.
What does DDP Specialty Electronic Materials US 9 make?
1 molecule is on record against DDP Specialty Electronic Materials US 9, including Simethicone. Each links through to that molecule's full manufacturer list.
Which regulators recognise DDP Specialty Electronic Materials US 9'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

  • The most recent inspection outcome was NAI, on 16 April 2025.

Comparable suppliers

RioCare India shares 1 molecule Basildon Chemical shares 1 molecule Aaa Pharmaceuticals also in United States Aarkish Pharmaceuticals NJ also in United States Abbott Laboratories also in United States

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