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Ciclopirox Olamine

NDC 51672-1318, ciclopirox olamine, cream, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-1318
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CREAM
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076790
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1318 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • CICLOPIROX OLAMINE7.7 mg/g

Pharmacologic classes

Decreased DNA Replication [PE]; Decreased Protein Synthesis [PE]; Decreased RNA Replication [PE]; Protein Synthesis Inhibitors [MoA]

Package NDCNDC-11Package
51672-1318-1516721318011 TUBE in 1 CARTON (51672-1318-1) / 15 g in 1 TUBE
51672-1318-2516721318021 TUBE in 1 CARTON (51672-1318-2) / 30 g in 1 TUBE
51672-1318-8516721318081 TUBE in 1 CARTON (51672-1318-8) / 90 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7fa4032e-a819-4574-b484-c57aaf1c5b01

  • NADAC price for package 51672131801

    GET /v1/drugs/nadac/51672131801

  • NADAC price for package 51672131802

    GET /v1/drugs/nadac/51672131802

  • NADAC price for package 51672131808

    GET /v1/drugs/nadac/51672131808

Use it

Look up 51672-1318 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1318 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-1318. 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.