Register entry

FRANCOPIA

Data as of · How to read this entry

Registered sites
0
Active NDC listings
7
Live patents
0
Countries
0
Catalogue

Drug listings by form and route

7

7 active NDC listings: 7 bulk ingredient. By marketing category: BULK INGREDIENT 7.

Dosage formNDCs
powder7
RouteNDCs
Labeller name on the listingNDCs
francopia7
Catalogue

Marketed products

7
BrandGeneric nameForm / routeNDC
-APOMORPHINE HYDROCHLORIDEpowder52465-104BULK INGREDIENT
-APOMORPHINE HYDROCHLORIDEpowder52465-105BULK INGREDIENT
-NALBUPHINE HYDROCHLORIDEpowder52465-106BULK INGREDIENT
-NALOXONE HYDROCHLORIDEpowder52465-101BULK INGREDIENT
-NALOXONE HYDROCHLORIDEpowder52465-102BULK INGREDIENT
-NALOXONE HYDROCHLORIDEpowder52465-107BULK INGREDIENT
-NALTREXONE HYDROCHLORIDEpowder52465-103BULK INGREDIENT
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Other companies listing naloxone hydrochloride

Enquiry

Common questions

Is FRANCOPIA FDA approved?
FRANCOPIA holds no registered establishment of its own; 7 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does FRANCOPIA make?
7 products are listed under FRANCOPIA 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.