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Voriconazole

NDC 16714-198, Voriconazole, tablet, film coated, from NorthStar Rx LLC.

Product NDC
16714-198
Status
Listed
Labeler
NorthStar Rx LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA206837
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/16714-198 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VORICONAZOLE50 mg/1

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
16714-198-011671401980130 TABLET, FILM COATED in 1 BOTTLE (16714-198-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b38165a5-d8d4-4579-a49a-fbe92e764089

  • NADAC price for package 16714019801

    GET /v1/drugs/nadac/16714019801

Use it

Look up 16714-198 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/16714-198 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 16714-198. 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.