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NDC 51672-2100, Butenafine Hydrochloride, cream, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-2100
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CREAM
Route
TOPICAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA205181
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-2100 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUTENAFINE HYDROCHLORIDE10 mg/g

Pharmacologic classes

Benzylamine Antifungal [EPC]; Benzylamines [CS]

Package NDCNDC-11Package
51672-2100-1516722100011 TUBE in 1 CARTON (51672-2100-1) / 15 g in 1 TUBE
51672-2100-2516722100021 TUBE in 1 CARTON (51672-2100-2) / 30 g in 1 TUBE
51672-2100-8516722100081 TUBE in 1 CARTON (51672-2100-8) / 12 g in 1 TUBE
51672-2100-9516722100091 TUBE in 1 CARTON (51672-2100-9) / 24 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 51672210002

    GET /v1/drugs/nadac/51672210002
  • NADAC price for package 51672210008

    GET /v1/drugs/nadac/51672210008

Use it

Look up 51672-2100 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-2100 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-2100. 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.