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Naftifine Hydrochloride

NDC 51672-1362, Naftifine Hydrochloride, cream, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-1362
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
CREAM
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205975
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1362 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NAFTIFINE HYDROCHLORIDE10 mg/g

Pharmacologic classes

Allylamine Antifungal [EPC]; Allylamine [CS]

Package NDCNDC-11Package
51672-1362-1516721362011 TUBE in 1 CARTON (51672-1362-1) / 15 g in 1 TUBE
51672-1362-2516721362021 TUBE in 1 CARTON (51672-1362-2) / 30 g in 1 TUBE
51672-1362-3516721362031 TUBE in 1 CARTON (51672-1362-3) / 60 g in 1 TUBE
51672-1362-8516721362081 TUBE in 1 CARTON (51672-1362-8) / 90 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d50961c2-e97f-4583-91d6-7cafd25a8c3d

  • NADAC price for package 51672136203

    GET /v1/drugs/nadac/51672136203

Use it

Look up 51672-1362 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1362 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-1362. 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.