Register entry

Boehringer Ingelheim Promeco S.A. de C.V.

Data as of · How to read this entry

Registered sites
1
Active NDC listings
3
Live patents
0
Countries
1
Base
Mexico
Authorisation

Registered operations

Analytical testing1Labelling1Finished drug manufacture1Packaging1Relabelling1Repackaging1
Sites

Registered establishments

1
EstablishmentAddressRegistered forFEI / DUNS
Boehringer Ingelheim Promeco S.A. de C.V.Maiz No. 49, Barrio Xaltocan, Xochimilco, Mexico City, DF 16090, Mexico (MEX)Analytical testing, Labelling, Finished drug manufacture, Packaging, Relabelling, Repackaging1000183111812579472
Catalogue

Drug listings by form and route

3

3 active NDC listings: 3 drug for further processing. By marketing category: DRUG FOR FURTHER PROCESSING 3.

Dosage formNDCs
tablet3
RouteNDCs
Labeller name on the listingNDCs
boehringer ingelheim promeco s.a. de c.v.3
Catalogue

Marketed products

3
BrandGeneric nameForm / routeNDC
-Linsgliptintablet64674-999DRUG FOR FURTHER PROCESSING
-empagliflozintablet64674-150DRUG FOR FURTHER PROCESSING
-empagliflozintablet64674-160DRUG FOR FURTHER PROCESSING
Neighbours

Registered in the same town

2
Compare

Comparable companies in Mexico

Enquiry

Common questions

Is Boehringer Ingelheim Promeco S.A. de C.V. FDA approved?
Boehringer Ingelheim Promeco S.A. de C.V. holds 1 FDA-registered establishment in Mexico. 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 Boehringer Ingelheim Promeco S.A. de C.V.'s drugs manufactured?
The FDA register lists Mexico City. Registered operations: analytical testing, labelling, finished drug manufacture, packaging, relabelling, repackaging.
What drugs does Boehringer Ingelheim Promeco S.A. de C.V. make?
3 products are listed under Boehringer Ingelheim Promeco S.A. de C.V. in the openFDA NDC Directory, most often as 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.