Cefixime
NDC 65862-752, cefixime, powder, for suspension, from Aurobindo Pharma Limited.
- Product NDC
- 65862-752
- Status
- Listed
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA204835
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/65862-752 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CEFIXIME200 mg/5mL
Pharmacologic classes
Cephalosporin Antibacterial [EPC]; Cephalosporins [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 65862-752-50 | 65862075250 | 50 mL in 1 BOTTLE (65862-752-50) |
| 65862-752-75 | 65862075275 | 75 mL in 1 BOTTLE (65862-752-75) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/068e6edd-a5fe-40d8-8dcf-ac82b78dced4NADAC price for package 65862075250
GET /v1/drugs/nadac/65862075250
Use it
Look up 65862-752 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/65862-752 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 65862-752. 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.