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Oralone

NDC 51672-1335, Triamcinolone Acetonide, paste, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-1335
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
PASTE
Route
DENTAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA070730
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1335 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • TRIAMCINOLONE ACETONIDE1 mg/g

Pharmacologic classes

Corticosteroid Hormone Receptor Agonists [MoA]; Corticosteroid [EPC]

Package NDCNDC-11Package
51672-1335-5516721335051 TUBE in 1 CARTON (51672-1335-5) / 5 g in 1 TUBE
51672-1335-8516721335081 TUBE in 1 CARTON (51672-1335-8) / 7.5 g in 1 TUBE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ac1e2116-795e-4c20-974d-11fa07cf0fa7

Use it

Look up 51672-1335 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-1335 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-1335. 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.