Details for New Drug Application (NDA): 219234
The generic ingredient in PRUCALOPRIDE SUCCINATE is prucalopride succinate. There is one drug master file entry for this compound. Nineteen suppliers are listed for this compound. Additional details are available on the prucalopride succinate profile page.
Summary for 219234
| Tradename: | PRUCALOPRIDE SUCCINATE |
| Applicant: | Alembic |
| Ingredient: | prucalopride succinate |
| Patents: | 0 |
Pharmacology for NDA: 219234
| Mechanism of Action | Serotonin 4 Receptor Agonists |
Suppliers and Packaging for NDA: 219234
| Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
|---|---|---|---|---|---|---|---|---|
| PRUCALOPRIDE SUCCINATE | prucalopride succinate | TABLET;ORAL | 219234 | ANDA | Alembic Pharmaceuticals Limited | 46708-077 | 46708-077-30 | 30 TABLET, FILM COATED in 1 BOTTLE (46708-077-30) |
| PRUCALOPRIDE SUCCINATE | prucalopride succinate | TABLET;ORAL | 219234 | ANDA | Alembic Pharmaceuticals Limited | 46708-078 | 46708-078-30 | 30 TABLET, FILM COATED in 1 BOTTLE (46708-078-30) |
Profile for product number 001
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 1MG BASE | ||||
| Approval Date: | Jul 27, 2026 | TE: | AB | RLD: | No | ||||
Profile for product number 002
| Active Rx/OTC/Discontinued: | RX | Dosage: | TABLET;ORAL | Strength | EQ 2MG BASE | ||||
| Approval Date: | Jul 27, 2026 | TE: | AB | RLD: | No | ||||
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