Is Valdepharm FDA approved?

Valdepharm holds 1 FDA-registered establishment in France. 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 Valdepharm's drugs manufactured?

The FDA register lists VAL DE REUIL CEDEX. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, finished drug manufacture, packaging, sterilize.

What drugs does Valdepharm make?

17 products are listed under Valdepharm 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.

Valdepharm

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

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Registered sites: 1
Active NDC listings: 17
Live patents: 0
Countries: 1
Base: France

Authorisation

Registered operations

Analytical testing1Active ingredient (API) manufacture1Labelling1Finished drug manufacture1Packaging1sterilize1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Valdepharm	PARC INDUSTRIEL D INCARVILLE PARC DE LA FRINGALE - CS10606, VAL DE REUIL CEDEX, NORMANDIE 27106, France (FRA)	Analytical testing, Active ingredient (API) manufacture, Labelling, Finished drug manufacture, Packaging, sterilize	3000538143260128560

Catalogue

Drug listings by form and route

17 active NDC listings: 17 bulk ingredient. By marketing category: BULK INGREDIENT 16, BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING 1.

Dosage form	NDCs
powder	17

Route	NDCs

Labeller name on the listing	NDCs
valdepharm	17

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	Atrenogest	powder	24823-913BULK INGREDIENT
-	Avibactam Sodium	powder	24823-915BULK INGREDIENT
-	Estradiol Cypionate	powder	24823-916BULK INGREDIENT
-	Estradiol Hemihydrate	powder	24823-903BULK INGREDIENT
-	Estradiol Valerate	powder	24823-905BULK INGREDIENT
-	Estradiol benzoate	powder	24823-902BULK INGREDIENT
-	Estradiol benzoate coarse grade	powder	24823-901BULK INGREDIENT
-	Estradiol hemihydrate micronized fine grade	powder	24823-904BULK INGREDIENT
-	Estradiol valerate micronized fine grade	powder	24823-906BULK INGREDIENT
-	Hydrocortisone hemisuccinate monohydrate	powder	24823-907BULK INGREDIENT
-	Norethindrone acetate	powder	24823-908BULK INGREDIENT
-	Norethindrone acetate micronized	powder	24823-909BULK INGREDIENT
-	Norethindrone micronized	powder	24823-910BULK INGREDIENT
-	Relebactam	powder	24823-154BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
-	Tenapanor	powder	24823-914BULK INGREDIENT
-	Trazodone hydrochloride	powder	24823-911BULK INGREDIENT
-	Trenbolone acetate	powder	24823-912BULK INGREDIENT

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Enquiry

Common questions

Is Valdepharm FDA approved?: Valdepharm holds 1 FDA-registered establishment in France. 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 Valdepharm's drugs manufactured?: The FDA register lists VAL DE REUIL CEDEX. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, finished drug manufacture, packaging, sterilize.
What drugs does Valdepharm make?: 17 products are listed under Valdepharm 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.