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voriconazole

NDC 70436-230, voriconazole, powder, for suspension, from Slate Run Pharmaceuticals, LLC.

Product NDC
70436-230
Status
Listed
Labeler
Slate Run Pharmaceuticals, LLC
Dosage form
POWDER, FOR SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216805
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70436-230 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • VORICONAZOLE40 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
70436-230-39704360230391 BOTTLE in 1 CARTON (70436-230-39) / 75 mL in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2b262849-9a29-44a2-9b9d-2378f771379c

  • NADAC price for package 70436023039

    GET /v1/drugs/nadac/70436023039

Use it

Look up 70436-230 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70436-230 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70436-230. 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.