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Triasil

NDC 59088-730, Triamcinolone Acetonide, kit, from PureTek Corporation.

Product NDC
59088-730
Status
Listed
Labeler
PureTek Corporation
Dosage form
KIT
Route
—
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
UNAPPROVED DRUG OTHER
Application
—
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59088-730 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

None listed.

Package NDCNDC-11Package
59088-730-00590880730001 KIT in 1 KIT (59088-730-00) * 1 TUBE in 1 CARTON (45802-055-36) / 80 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dcf6c630-6f5d-3d2f-e053-2995a90ad812

Use it

Look up 59088-730 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59088-730 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59088-730. 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.