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PredniSONE Tablets, USP, 20 mg

NDC 72789-500, PredniSONE, tablet, from PD-Rx Pharmaceuticals, Inc..

Product NDC
72789-500
Status
Listed
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212629
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72789-500 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PREDNISONE20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
72789-500-217278905002121 TABLET in 1 BOTTLE, PLASTIC (72789-500-21)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3befbdc5-7d20-41b6-ad80-98e1c6b8caf5

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=72789-500

Use it

Look up 72789-500 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72789-500 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72789-500. 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.