Suppliers / Abbott Healthcare Products

Abbott Healthcare Products

Netherlands Updated 9 July 2026

Abbott Healthcare Products is an API and finished-dose manufacturer based in Netherlands. It holds 2 valid CEPs across a filed portfolio of 2 molecules. Its filings concentrate with RAMA (GE), SFDA (Saudi Arabia) and MPA (SE). Its GMP standing is certified by EMA.

0
active US DMFs
2
valid CEPs
1
registered plants
21
filings across 4 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Weesp, Netherlands Not on file

What they file, and where

Molecule Regulators Docs
Lactulose EDQM 1
Medroxyprogesterone Acetate EDQM 1

Also appears on these molecule pages

Fluvoxamine finished dose Lactulose API Medroxyprogesterone API

Filings and GMP by regulator

Regulator Filings GMP certificates
RAMA (GE) 13 None
SFDA (Saudi Arabia) 4 None
MPA (SE) 2 None
NMPA (CN) 2 None
EMA None 1

Questions about Abbott Healthcare Products

Does Abbott Healthcare Products hold a US DMF or a CEP?
Abbott Healthcare Products 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 Abbott Healthcare Products manufacture?
1 registered site is on record, in Netherlands (Weesp). Every site is listed on this page with the register it came from.
What does Abbott Healthcare Products make?
2 molecules are on record against Abbott Healthcare Products, including Lactulose and Medroxyprogesterone Acetate. Each links through to that molecule's full manufacturer list.
Which regulators recognise Abbott Healthcare Products's GMP?
Current GMP certificates are on record from EMA. 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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Comparable suppliers

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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