Is Dow Benelux B.V. FDA approved?

Dow Benelux B.V. holds 1 FDA-registered establishment in the Netherlands. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.

Where are Dow Benelux B.V.'s drugs manufactured?

The FDA register lists Hoek. Registered operations: active ingredient (API) manufacture.

What drugs does Dow Benelux B.V. make?

8 products are listed under Dow Benelux B.V. in the openFDA NDC Directory, most often as powder; granule. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Dow Benelux B.V.

Data as of 24 Sept 2026 · How to read this entry

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Registered sites: 1
Active NDC listings: 8
Live patents: 0
Countries: 1
Base: Netherlands

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Dow Benelux B.V.	Herbert.H. Dowweg 5, Hoek, 4542 NM, Netherlands (NLD)	Active ingredient (API) manufacture	3001555205405388836

Catalogue

Drug listings by form and route

8 active NDC listings: 8 bulk ingredient. By marketing category: BULK INGREDIENT 8.

Dosage form	NDCs
powder	6
granule	2

Route	NDCs

Labeller name on the listing	NDCs
dow benelux b.v.	8

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	Polyethylene Glycol 3350	granule	87289-3351BULK INGREDIENT
-	Polyethylene Glycol 3350	powder	87289-3352BULK INGREDIENT
-	Polyethylene Glycol 3350	powder	87289-3353BULK INGREDIENT
-	Polyethylene Glycol 3350	powder	87289-3354BULK INGREDIENT
-	Polyethylene Glycol 3350	granule	87289-3355BULK INGREDIENT
-	Polyethylene Glycol 4000	powder	87289-4001BULK INGREDIENT
-	Polyethylene Glycol 4000	powder	87289-4002BULK INGREDIENT
-	Polyethylene Glycol 4000	powder	87289-4003BULK INGREDIENT

Compare

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Enquiry

Common questions

Is Dow Benelux B.V. FDA approved?: Dow Benelux B.V. holds 1 FDA-registered establishment in the Netherlands. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
Where are Dow Benelux B.V.'s drugs manufactured?: The FDA register lists Hoek. Registered operations: active ingredient (API) manufacture.
What drugs does Dow Benelux B.V. make?: 8 products are listed under Dow Benelux B.V. in the openFDA NDC Directory, most often as powder; granule. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.