HYDROXYUREA
NDC 70069-820, HYDROXYUREA, capsule, from Somerset Therapeutics, LLC.
- Product NDC
- 70069-820
- Status
- Listed
- Labeler
- Somerset Therapeutics, LLC
- Dosage form
- CAPSULE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA218021
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/70069-820 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- HYDROXYUREA500 mg/1
Pharmacologic classes
Antimetabolite [EPC]; Urea [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70069-820-01 | 70069082001 | 100 CAPSULE in 1 BOTTLE (70069-820-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/9752a347-b42c-44d5-8fd1-c538f7f239dcNADAC price for package 70069082001
GET /v1/drugs/nadac/70069082001
Use it
Look up 70069-820 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70069-820 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70069-820. 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.