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Naftin

NDC 54766-772, Naftifine Hydrochloride, gel, from Sebela Pharmaceuticals Inc..

Product NDC
54766-772
Status
Listed
Labeler
Sebela Pharmaceuticals Inc.
Dosage form
GEL
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA204286
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/54766-772 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NAFTIFINE HYDROCHLORIDE2 g/100g

Pharmacologic classes

Allylamine Antifungal [EPC]; Allylamine [CS]

Package NDCNDC-11Package
54766-772-45547660772451 TUBE in 1 CARTON (54766-772-45) / 45 g in 1 TUBE
54766-772-60547660772601 TUBE in 1 CARTON (54766-772-60) / 60 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6645994a-ecb3-277b-e053-2a91aa0a81e5

Use it

Look up 54766-772 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/54766-772 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 54766-772. 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.