Is Moehs Catalana SL FDA approved?

Moehs Catalana SL holds 1 FDA-registered establishment in Spain. 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 Moehs Catalana SL's drugs manufactured?

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

What drugs does Moehs Catalana SL make?

20 products are listed under Moehs Catalana SL 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.

Moehs Catalana SL

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

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Registered sites: 1
Active NDC listings: 20
Labeller names: 2
Live patents: 0
Countries: 1
Base: Spain

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Moehs Catalana SL	Calle Cesar Martinell I Brunet, 12-A (PG IND RUBI SUR), Rubi, Barcelona 08191, Spain (ESP)	Active ingredient (API) manufacture	3002807632460021629

Catalogue

Drug listings by form and route

20 active NDC listings: 20 bulk ingredient. By marketing category: BULK INGREDIENT 20.

Dosage form	NDCs
powder	20

Route	NDCs

Labeller name on the listing	NDCs
moehs catalana sl	19
moehs catalana, s.l.	1

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	ACETYLCYSTEINE	powder	52932-0704BULK INGREDIENT
-	AMANTADINE HYDROCHLORIDE	powder	52932-0707BULK INGREDIENT
-	AMLODIPINE BESYLATE	powder	52932-0723BULK INGREDIENT
-	BISOPROLOL FUMARATE	powder	52932-0720BULK INGREDIENT
-	BUPIVACAINE HYDROCHLORIDE	powder	52932-0729BULK INGREDIENT
-	CARVEDILOL	powder	52932-0726BULK INGREDIENT
-	LANSOPRAZOLE	powder	52932-0730BULK INGREDIENT
-	LIDOCAINE	powder	52932-0702BULK INGREDIENT
-	LIDOCAINE HYDROCHLORIDE	powder	52932-0701BULK INGREDIENT
-	MEPIVACAINE HYDROCHLORIDE	powder	52932-0731BULK INGREDIENT
-	METOPROLOL SUCCINATE	powder	52932-0713BULK INGREDIENT
-	METOPROLOL TARTRATE	powder	52932-0710BULK INGREDIENT
-	METOPROLOL TARTRATE DS/IP	powder	52932-0721BULK INGREDIENT
-	Metoprolol Tartrate	powder	52932-0743BULK INGREDIENT
-	NIFEDIPINE	powder	52932-0711BULK INGREDIENT
-	PYRANTEL PAMOATE	powder	52932-0714BULK INGREDIENT
-	SOTALOL HYDROCHLORIDE	powder	52932-0715BULK INGREDIENT
-	SUMATRIPTAN	powder	52932-0733BULK INGREDIENT
-	Sumatriptan Succinate	powder	52932-0727BULK INGREDIENT
-	Triamterene	powder	52932-0703BULK INGREDIENT

Neighbours

Registered in the same town

Moehs Iberica SLRubi, ESP

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Enquiry

Common questions

Is Moehs Catalana SL FDA approved?: Moehs Catalana SL holds 1 FDA-registered establishment in Spain. 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 Moehs Catalana SL's drugs manufactured?: The FDA register lists Rubi. Registered operations: active ingredient (API) manufacture.
What drugs does Moehs Catalana SL make?: 20 products are listed under Moehs Catalana SL 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.