YONSA
NDC 47335-401, abiraterone acetate, tablet, from Sun Pharmaceutical Industries, Inc..
- Product NDC
- 47335-401
- Status
- Listed
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA210308
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/47335-401 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- ABIRATERONE ACETATE125 mg/1
Pharmacologic classes
Cytochrome P450 17A1 Inhibitor [EPC]; Cytochrome P450 17A1 Inhibitors [MoA]; Cytochrome P450 2C8 Inhibitors [MoA]; Cytochrome P450 2D6 Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 47335-401-81 | 47335040181 | 120 TABLET in 1 BOTTLE, PLASTIC (47335-401-81) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/b8967e10-f768-47ce-ac9e-2324c8390132
Use it
Look up 47335-401 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/47335-401 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 47335-401. 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.