Prucalopride
NDC 60505-4807, Prucalopride, tablet, film coated, from Apotex Corp..
- Product NDC
- 60505-4807
- Status
- Listed
- Labeler
- Apotex Corp.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA218977
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/60505-4807 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PRUCALOPRIDE SUCCINATE2 mg/1
Pharmacologic classes
Serotonin 4 Receptor Agonists [MoA]; Serotonin-4 Receptor Agonist [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 60505-4807-3 | 60505480703 | 30 TABLET, FILM COATED in 1 BOTTLE (60505-4807-3) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/01dcea95-b391-79da-bbfe-412f39022e9aNADAC price for package 60505480703
GET /v1/drugs/nadac/60505480703
Use it
Look up 60505-4807 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/60505-4807 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 60505-4807. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.