Siklos
NDC 71770-120, hydroxyurea, tablet, film coated, from Medunik.
- Product NDC
- 71770-120
- Status
- Listed
- Labeler
- Medunik
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA208843
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/71770-120 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- HYDROXYUREA1000 mg/1
Pharmacologic classes
Antimetabolite [EPC]; Urea [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 71770-120-30 | 71770012030 | 1 BOTTLE in 1 CARTON (71770-120-30) / 30 TABLET, FILM COATED in 1 BOTTLE |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/76957c0d-0f98-4376-bb06-eee651adc09dNADAC price for package 71770012030
GET /v1/drugs/nadac/71770012030
Use it
Look up 71770-120 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/71770-120 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 71770-120. 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.