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Fluconazole

NDC 72673-091, Fluconazole, powder, for suspension, from Zhejiang Poly Pharm. Co., Ltd..

Product NDC
72673-091
Status
Listed
Labeler
Zhejiang Poly Pharm. Co., Ltd.
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215738
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72673-091 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • FLUCONAZOLE40 mg/mL

Pharmacologic classes

Azole Antifungal [EPC]; Azoles [CS]; Cytochrome P450 2C19 Inhibitors [MoA]; Cytochrome P450 2C9 Inhibitors [MoA]; Cytochrome P450 3A4 Inhibitors [MoA]

Package NDCNDC-11Package
72673-091-14726730091141 BOTTLE in 1 CARTON (72673-091-14) / 35 mL in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2a3ba181-5baa-5942-e063-6294a90a82b2

Use it

Look up 72673-091 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72673-091 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72673-091. 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.