POLYMYXIN B
NDC 63323-321, POLYMYXIN B SULFATE, injection, powder, lyophilized, for solution, from Fresenius Kabi USA, LLC.
- Product NDC
- 63323-321
- Status
- Listed
- Labeler
- Fresenius Kabi USA, LLC
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAMUSCULAR, INTRATHECAL, INTRAVENOUS, OPHTHALMIC
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA065372
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/63323-321 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- POLYMYXIN B SULFATE500000 [USP'U]/1
Pharmacologic classes
Polymyxin-class Antibacterial [EPC]; Polymyxins [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 63323-321-10 | 63323032110 | 10 VIAL in 1 TRAY (63323-321-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (63323-321-01) |
| 63323-321-12 | 63323032112 | 10 VIAL in 1 TRAY (63323-321-12) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL (63323-321-02) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels?ndc=63323-321
Use it
Look up 63323-321 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/63323-321 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 63323-321. 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.