PROPOFOL
NDC 0409-0010, PROPOFOL, injection, emulsion, from Hospira, Inc..
- Product NDC
- 0409-0010
- Status
- Listed
- Labeler
- Hospira, Inc.
- Dosage form
- INJECTION, EMULSION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA077908
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0409-0010 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- PROPOFOL10 mg/mL
Pharmacologic classes
General Anesthesia [PE]; General Anesthetic [EPC]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 0409-0010-98 | 00409001098 | 10 VIAL, SINGLE-DOSE in 1 TRAY (0409-0010-98) / 100 mL in 1 VIAL, SINGLE-DOSE (0409-0010-97) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/28d7ba00-f824-4e55-139a-03f509c099db
Use it
Look up 0409-0010 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0409-0010 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0409-0010. 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.