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LULICONAZOLE

NDC 68682-850, LULICONAZOLE, cream, from Oceanside Pharmaceuticals.

Product NDC
68682-850
Status
Listed
Labeler
Oceanside Pharmaceuticals
Dosage form
CREAM
Route
TOPICAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA204153
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68682-850 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LULICONAZOLE10 mg/g

Pharmacologic classes

Azole Antifungal [EPC]; Azoles [CS]; Cytochrome P450 2C19 Inhibitors [MoA]

Package NDCNDC-11Package
68682-850-60686820850601 TUBE in 1 CARTON (68682-850-60) / 60 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7ccda3ba-9c98-468d-83c6-7f0cc7c88c33

Use it

Look up 68682-850 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68682-850 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68682-850. 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.