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SODIUM SULFACETAMIDE

NDC 71399-0480, SODIUM SULFACETAMIDE, liquid, from Akron Pharma Inc.

Product NDC
71399-0480
Status
Listed
Labeler
Akron Pharma Inc
Dosage form
LIQUID
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/71399-0480 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SULFACETAMIDE SODIUM100 mg/mL

Pharmacologic classes

Sulfonamide Antibacterial [EPC]; Sulfonamides [CS]

Package NDCNDC-11Package
71399-0480-271399048002360 mL in 1 BOTTLE (71399-0480-2)
71399-0480-671399048006480 mL in 1 BOTTLE (71399-0480-6)
71399-0480-871399048008240 mL in 1 BOTTLE (71399-0480-8)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ba08bf7c-5fdc-447a-b8de-3f319cee7e4e

Use it

Look up 71399-0480 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71399-0480 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71399-0480. 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.