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Voriconazole

NDC 0378-1626, voriconazole, tablet, film coated, from Mylan Pharmaceuticals Inc..

Product NDC
0378-1626
Status
Listed
Labeler
Mylan Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090547
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0378-1626 \
  -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
0378-1626-930037816269330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-1626-93)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/67c174da-41b8-4738-8a22-dd814b8e96b8

Use it

Look up 0378-1626 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0378-1626 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0378-1626. 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.