decitabine
NDC 47335-361, decitabine, kit, from Sun Pharmaceutical Industries, Inc..
- Product NDC
- 47335-361
- Status
- Listed
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- KIT
- Route
- —
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA205582
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/47335-361 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
None listed.
| Package NDC | NDC-11 | Package |
|---|---|---|
| 47335-361-41 | 47335036141 | 1 KIT in 1 CARTON (47335-361-41) * 10 mL in 1 VIAL, SINGLE-DOSE * 10 mL in 1 VIAL (47335-362-40) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/c155d6ba-9a16-406c-919e-65a149689ab9
Use it
Look up 47335-361 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/47335-361 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 47335-361. 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.