CEFIXIME
NDC 68180-405, CEFIXIME, powder, for suspension, from Lupin Pharmaceuticals, Inc..
- Product NDC
- 68180-405
- Status
- Listed
- Labeler
- Lupin Pharmaceuticals, Inc.
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA065129
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68180-405 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- CEFIXIME100 mg/5mL
Pharmacologic classes
Cephalosporin Antibacterial [EPC]; Cephalosporins [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68180-405-01 | 68180040501 | 50 mL in 1 BOTTLE (68180-405-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/6d68dbd9-7d75-4ff1-91db-79ff8ae879ec
Use it
Look up 68180-405 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68180-405 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68180-405. 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.