Propofol
NDC 0069-0248, Propofol, injection, emulsion, from Pfizer Laboratories Div Pfizer Inc.
- Product NDC
- 0069-0248
- Status
- Listed
- Labeler
- Pfizer Laboratories Div Pfizer Inc
- Dosage form
- INJECTION, EMULSION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA205576
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/0069-0248 \ -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 |
|---|---|---|
| 0069-0248-10 | 00069024810 | 10 VIAL in 1 CARTON (0069-0248-10) / 100 mL in 1 VIAL |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/3acf8e6c-827d-11e2-9e96-0800200c9a66Medicare Part B payment limits (ASP)
GET /v1/drugs/asp?ndc=0069-0248
Use it
Look up 0069-0248 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0069-0248 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0069-0248. 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.