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SULFACETAMIDE SODIUM, SULFUR

NDC 81542-202, SULFACETAMIDE SODIUM, SULFUR, solution, from Bantry Pharma, LLC.

Product NDC
81542-202
Status
Listed
Labeler
Bantry Pharma, LLC
Dosage form
SOLUTION
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/81542-202 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SULFUR50 mg/mL
  • SULFACETAMIDE SODIUM100 mg/mL

Pharmacologic classes

Sulfonamide Antibacterial [EPC]; Sulfonamides [CS]

Package NDCNDC-11Package
81542-202-1281542020212355 mL in 1 BOTTLE (81542-202-12)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f433db67-d8a6-320e-e053-2995a90aab52

Use it

Look up 81542-202 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/81542-202 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 81542-202. 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.