prucalopride
- Product NDC
- 70771-1899
- 11-digit product format
- 707711899
- Labeler code
- 70771
- Product ID
- 70771-1899_051f4f7e-88e8-4706-8183-dbd3f9d42d72
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prucalopride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA218056
- Marketing category
- ANDA
- Marketing start
- 2026-02-02
- Substance
- PRUCALOPRIDE SUCCINATE
- Active strength
- 1 mg/1
- Pharmacologic classes
- Serotonin 4 Receptor Agonists [MoA], Serotonin-4 Receptor Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- prucalopride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PRUCALOPRIDE SUCCINATE | 1 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4V2G75E1CK |
| Rxcui | 2107345, 2107353 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70771-1899-3 | prucalopride | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70771-1899-3 | 70771189903 | 30 TABLET, FILM COATED in 1 BOTTLE (70771-1899-3) | 2026-02-02 | No | No | Current |