Docetaxel
NDC 57884-3042, Docetaxel, injection, solution, concentrate, from Jiangsu Hengrui Pharmaceuticals Co., Ltd..
- Product NDC
- 57884-3042
- Status
- Listed
- Labeler
- Jiangsu Hengrui Pharmaceuticals Co., Ltd.
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA207252
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/57884-3042 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- DOCETAXEL80 mg/4mL
Pharmacologic classes
Microtubule Inhibition [PE]; Microtubule Inhibitor [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 57884-3042-1 | 57884304201 | 1 VIAL, GLASS in 1 CARTON (57884-3042-1) / 4 mL in 1 VIAL, GLASS |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/e488100d-6728-4f44-9282-f63a805b8e13
Use it
Look up 57884-3042 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/57884-3042 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 57884-3042. 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.