DOXOrubicin Hydrochloride
NDC 62756-827, DOXOrubicin Hydrochloride, injection, solution, from Sun Pharmaceutical Industries, Inc..
- Product NDC
- 62756-827
- Status
- Listed
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA091418
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/62756-827 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DOXORUBICIN HYDROCHLORIDE2 mg/mL
Pharmacologic classes
Anthracycline Topoisomerase Inhibitor [EPC]; Anthracyclines [CS]; Topoisomerase Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 62756-827-40 | 62756082740 | 1 VIAL, MULTI-DOSE in 1 BOX (62756-827-40) / 100 mL in 1 VIAL, MULTI-DOSE |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/6bcde92b-e584-4919-866a-68847ea201ba
Use it
Look up 62756-827 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/62756-827 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 62756-827. 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.