Is Bioventure Healthcare - FZE FDA approved?

Bioventure Healthcare - FZE holds 1 FDA-registered establishment in the UAE. 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 Bioventure Healthcare - FZE's drugs manufactured?

The FDA register lists National Industries Park. Registered operations: finished drug manufacture.

What drugs does Bioventure Healthcare - FZE make?

14 products are listed under Bioventure Healthcare - FZE in the openFDA NDC Directory, most often as capsule, liquid filled; capsule; tablet. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Bioventure Healthcare - FZE

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

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Registered sites: 1
Active NDC listings: 14
Live patents: 0
Countries: 1
Base: UAE

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Bioventure Healthcare - FZE	Plot No. TP020201, National Industries Park, Dubai, , United Arab Emirates (ARE)	Finished drug manufacture	3015366133557564562

Catalogue

Drug listings by form and route

14 active NDC listings: 14 drug for further processing. By marketing category: DRUG FOR FURTHER PROCESSING 14.

Dosage form	NDCs
capsule, liquid filled	8
capsule	4
tablet	2

Route	NDCs

Labeller name on the listing	NDCs
bioventure healthcare - fze	14

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	ACETAMINOPHEN, ASPIRIN, CAFFEINE	tablet	73056-001DRUG FOR FURTHER PROCESSING
-	ACETAMINOPHEN, CAFFEINE, PYRILAMINE MALEATE	tablet	73056-002DRUG FOR FURTHER PROCESSING
-	Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine Succinate, Phenylephrine Hydrochloride	capsule, liquid filled	73056-028DRUG FOR FURTHER PROCESSING
-	Acetaminophen, Dextromethorphan Hydrobromide, Doxylamine succinate	capsule, liquid filled	73056-023DRUG FOR FURTHER PROCESSING
-	Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride	capsule, liquid filled	73056-022DRUG FOR FURTHER PROCESSING
-	Acetaminophen, Guaifenesin, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride	capsule, liquid filled	73056-027DRUG FOR FURTHER PROCESSING
-	DEXTROMETHORPHAN HYDROBROMIDE	capsule	73056-019DRUG FOR FURTHER PROCESSING
-	DIPHENHYDRAMINE HYDROCHLORIDE	capsule	73056-016DRUG FOR FURTHER PROCESSING
-	DIPHENHYDRAMINE HYDROCHLORIDE	capsule	73056-018DRUG FOR FURTHER PROCESSING
-	DOCUSATE SODIUM	capsule	73056-017DRUG FOR FURTHER PROCESSING
-	Diphenhydramine Hydrochloride	capsule, liquid filled	73056-020DRUG FOR FURTHER PROCESSING
-	Simethicone	capsule, liquid filled	73056-021DRUG FOR FURTHER PROCESSING
-	Simethicone	capsule, liquid filled	73056-024DRUG FOR FURTHER PROCESSING
-	Simethicone	capsule, liquid filled	73056-025DRUG FOR FURTHER PROCESSING

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MDS GLOBAL FZE1 site · 1 NDC

Enquiry

Common questions

Is Bioventure Healthcare - FZE FDA approved?: Bioventure Healthcare - FZE holds 1 FDA-registered establishment in the UAE. 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 Bioventure Healthcare - FZE's drugs manufactured?: The FDA register lists National Industries Park. Registered operations: finished drug manufacture.
What drugs does Bioventure Healthcare - FZE make?: 14 products are listed under Bioventure Healthcare - FZE in the openFDA NDC Directory, most often as capsule, liquid filled; capsule; tablet. 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.