BEQALZI
NDC 72579-025, sonrotoclax, tablet, film coated, from BeOne Medicines USA, Inc..
- Product NDC
- 72579-025
- Status
- Listed
- Labeler
- BeOne Medicines USA, Inc.
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA
- Application
- NDA220711
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/72579-025 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SONROTOCLAX20 mg/1
| Package NDC | NDC-11 | Package |
|---|---|---|
| 72579-025-01 | 72579002501 | 1 BLISTER PACK in 1 CARTON (72579-025-01) / 11 TABLET, FILM COATED in 1 BLISTER PACK |
| 72579-025-02 | 72579002502 | 1 BLISTER PACK in 1 CARTON (72579-025-02) / 14 TABLET, FILM COATED in 1 BLISTER PACK |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/ff684558-e9cb-46de-a8bf-f4d79093df7a
Use it
Look up 72579-025 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/72579-025 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 72579-025. 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.