SODIUM SULFACETAMIDE AND SULFUR
NDC 44523-748, Sodium Sulfacetamide 9.8% and Sulfur 4.8%, emulsion, from BioComp Pharma, Inc..
- Product NDC
- 44523-748
- Status
- Listed
- Labeler
- BioComp Pharma, Inc.
- Dosage form
- EMULSION
- Route
- TOPICAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- UNAPPROVED DRUG OTHER
- Application
- —
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/44523-748 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- SULFACETAMIDE SODIUM98 mg/g
- SULFUR48 mg/g
Pharmacologic classes
Sulfonamide Antibacterial [EPC]; Sulfonamides [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 44523-748-10 | 44523074810 | 285 g in 1 BOTTLE, PLASTIC (44523-748-10) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/1ba8bb47-6f7a-28ec-e063-6394a90a8eb3
Use it
Look up 44523-748 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/44523-748 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 44523-748. 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.