Skip to content
healthcare.dev
Get a free key

Naftifine Hydrochloride

NDC 51672-1376, Naftifine Hydrochloride, gel, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-1376
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
GEL
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208201
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1376 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NAFTIFINE HYDROCHLORIDE20 mg/g

Pharmacologic classes

Allylamine Antifungal [EPC]; Allylamine [CS]

Package NDCNDC-11Package
51672-1376-3516721376031 TUBE in 1 CARTON (51672-1376-3) / 60 g in 1 TUBE
51672-1376-6516721376061 TUBE in 1 CARTON (51672-1376-6) / 45 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/92d3ec30-2176-49cd-8a70-668ef65e7663

  • NADAC price for package 51672137603

    GET /v1/drugs/nadac/51672137603

  • NADAC price for package 51672137606

    GET /v1/drugs/nadac/51672137606

Use it

Look up 51672-1376 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1376 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-1376. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Get a free keyNDC docsConnect the MCP server

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.