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Sodium Sulfacetamide and Sulfer Emulsion

NDC 73352-750, Sodium Sulfacetamide and Sulfer, emulsion, from Trifluent Pharma.

Product NDC
73352-750
Status
Listed
Labeler
Trifluent Pharma
Dosage form
EMULSION
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/73352-750 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SULFACETAMIDE SODIUM100 mg/mL
  • SULFUR10 mg/mL

Pharmacologic classes

Sulfonamide Antibacterial [EPC]; Sulfonamides [CS]

Package NDCNDC-11Package
73352-750-0173352075001177 mL in 1 BOTTLE (73352-750-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/40601d03-aea0-b0a6-e063-6394a90a1698

Use it

Look up 73352-750 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/73352-750 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 73352-750. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.