Drug

Who makes prucalopride?

17 companies list prucalopride as a human prescription drug, including under the names MOTEGRITY. Forms: tablet; tablet, film coated. Routes: oral.

Labellers from the openFDA NDC Directory. A labeller is the firm named on the label, not necessarily the site that made the product, and a listing is not an FDA approval. Data as of 24 Sept 2026. Methodology

Companies listing prucalopride

CompanyFormsApplicationNDCsRegistered sites
Alembic Pharmaceuticals LimitedIndiatablet, film coatedANDAANDA21923447
Lupin LimitedIndiatablet, film coatedANDAANDA218847214
Zydus Lifesciences LimitedIndiatablet, film coatedANDAANDA218056212
CIPLA PHARMACEUTICALS LIMITEDIndiatablet, film coatedANDAANDA21879527
Takeda Pharmaceuticals U.S.A., Inc.Germanytablet, film coatedNDANDA21016627
Apotex Inc.Canadatablet, film coatedANDAANDA21897726
Sandoz Industrial Products S.AAustriatablet, film coatedANDAANDA21896325
SpecGx LLCUnited Statestablet, film coatedANDAANDA21919325
Hikma Pharmaceuticals USA Inc.United Statestablet, film coatedANDAANDA21766224
Ajanta Pharma LimitedIndiatabletANDAANDA21922022
ANI Pharmaceuticals, Inc.United StatestabletANDAANDA21849221
Camber Pharmaceuticals, Inc.United Statestablet, film coatedANDAANDA21916021
Amneal Pharmaceuticals NY LLCtablet, film coatedANDAANDA21881220
AvKAREtablet, film coatedANDAANDA21897720
Novadoz Pharmaceuticals LLCtablet, film coatedANDAANDA21817720
SKG Pharma Inc.tablet, film coatedANDAANDA21881220
Viona Pharmaceuticals Inc.tablet, film coatedANDAANDA21805620
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Common questions

Who makes prucalopride?
17 companies list prucalopride as a human prescription drug in the openFDA NDC Directory, led by Alembic Pharmaceuticals Limited, Lupin Limited, Zydus Lifesciences Limited, CIPLA PHARMACEUTICALS LIMITED, Takeda Pharmaceuticals U.S.A., Inc.. Each is the labeller, the firm named on the label; the product may be made at a site registered to another company.
Is there a generic MOTEGRITY?
16 companies list prucalopride under an abbreviated new drug application (ANDA), the application type used for generics, and 1 under an NDA or BLA. Listing status is from the NDC Directory; it is not a statement of availability.