Propofol Injectable Emulsion
NDC 43598-548, Propofol Injectable Emulsion, injection, emulsion, from Dr. Reddy's Laboratories, Inc..
- Product NDC
- 43598-548
- Status
- Listed
- Labeler
- Dr. Reddy's Laboratories, Inc.
- Dosage form
- INJECTION, EMULSION
- Route
- INTRAVENOUS
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA205067
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/43598-548 \ -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 |
|---|---|---|
| 43598-548-21 | 43598054821 | 20 VIAL in 1 CARTON (43598-548-21) / 50 mL in 1 VIAL (43598-548-50) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/800646b8-83a8-01d9-3dc8-bb2ddcb8570cMedicare Part B payment limits (ASP)
GET /v1/drugs/asp?ndc=43598-548
Use it
Look up 43598-548 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/43598-548 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 43598-548. 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.