Is B.V. KATWIJK CHEMIE FDA approved?

B.V. KATWIJK CHEMIE 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 B.V. KATWIJK CHEMIE's drugs manufactured?

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

What drugs does B.V. KATWIJK CHEMIE make?

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

B.V. KATWIJK CHEMIE

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

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Registered sites: 1
Active NDC listings: 13
Labeller names: 4
Live patents: 0
Countries: 1
Base: Netherlands

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
B.V. KATWIJK CHEMIE	Snijderstraat 6, Katwijk ZH, 2222, Netherlands (NLD)	Active ingredient (API) manufacture	1000173675406037531

Catalogue

Drug listings by form and route

13 active NDC listings: 13 bulk ingredient. By marketing category: BULK INGREDIENT 12, BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING 1.

Dosage form	NDCs
powder	13

Route	NDCs

Labeller name on the listing	NDCs
b.v. katwijk chemie	10
b.v katwijk chemie	1
b.v. katwijk chemie	1
katwijk chemie bv	1

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	DEFERIPRONE	powder	17349-0023BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-	DIVALPROEX SODIUM	powder	17349-0011BULK INGREDIENT
-	ETHOSUXIMIDE	powder	17349-0006BULK INGREDIENT
-	OXAPROZIN	powder	17349-0008BULK INGREDIENT
-	PHENYTOIN	powder	17349-0007BULK INGREDIENT
-	PHENYTOIN SODIUM	powder	17349-0004BULK INGREDIENT
-	SULFACETAMIDE	powder	17349-0002BULK INGREDIENT
-	SULFACETAMIDE SODIUM	powder	17349-0001BULK INGREDIENT
-	SULFACETAMIDE SODIUM	powder	17349-0022BULK INGREDIENT
-	Sodium Valproate Crystals	powder	17349-0009BULK INGREDIENT
-	Sodium Valproate Powder	powder	17349-0020BULK INGREDIENT
-	Sulfacetamide Sodium Crystals	powder	17349-0010BULK INGREDIENT
-	VALPROIC ACID	powder	17349-0005BULK INGREDIENT

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Enquiry

Common questions

Is B.V. KATWIJK CHEMIE FDA approved?: B.V. KATWIJK CHEMIE 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 B.V. KATWIJK CHEMIE's drugs manufactured?: The FDA register lists Katwijk ZH. Registered operations: active ingredient (API) manufacture.
What drugs does B.V. KATWIJK CHEMIE make?: 13 products are listed under B.V. KATWIJK CHEMIE in the openFDA NDC Directory, most often as powder. 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.