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PredniSONE

NDC 0054-8739, PredniSONE, tablet, from Hikma Pharmaceuticals USA Inc..

Product NDC
0054-8739
Status
Listed
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA080352
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0054-8739 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PREDNISONE1 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
0054-8739-250005487392510 BLISTER PACK in 1 CARTON (0054-8739-25) / 10 TABLET in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3115aef0-fd50-4ec8-a064-3effb695f3f2

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=0054-8739

Use it

Look up 0054-8739 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0054-8739 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0054-8739. 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.