prucalopride
NDC 70771-1900, prucalopride, tablet, film coated, from Zydus Lifesciences Limited.
- Product NDC
- 70771-1900
- Status
- Listed
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA218056
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1900 \ -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 |
|---|---|---|
| 70771-1900-3 | 70771190003 | 30 TABLET, FILM COATED in 1 BOTTLE (70771-1900-3) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/da37395d-0a05-4fdc-ab5c-eb7caed62bf1
Use it
Look up 70771-1900 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1900 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70771-1900. 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.