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Naftifine Hydrochloride

NDC 51672-1368, Naftifine Hydrochloride, cream, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-1368
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CREAM
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206901
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1368 \
  -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
51672-1368-2516721368021 TUBE in 1 CARTON (51672-1368-2) / 30 g in 1 TUBE
51672-1368-3516721368031 TUBE in 1 CARTON (51672-1368-3) / 60 g in 1 TUBE
51672-1368-6516721368061 TUBE in 1 CARTON (51672-1368-6) / 45 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a740fc0d-45b3-411f-9dfd-f3d637b8a95f

  • NADAC price for package 51672136803

    GET /v1/drugs/nadac/51672136803

  • NADAC price for package 51672136806

    GET /v1/drugs/nadac/51672136806

Use it

Look up 51672-1368 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1368 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-1368. 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.