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PredniSONE Tablets, USP, 20 mg

NDC 63561-0122, PredniSONE, tablet, from Granulation Technology, Inc..

Product NDC
63561-0122
Status
Listed
Labeler
Granulation Technology, 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/63561-0122 \
  -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
63561-0122-163561012201100 TABLET in 1 BOTTLE (63561-0122-1)
63561-0122-2635610122021000 TABLET in 1 BOTTLE (63561-0122-2)
63561-0122-563561012205500 TABLET in 1 BOTTLE (63561-0122-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a173fcbb-99be-4b3e-a3a4-4e9ae04ad83f

  • NADAC price for package 63561012201

    GET /v1/drugs/nadac/63561012201

  • NADAC price for package 63561012202

    GET /v1/drugs/nadac/63561012202

  • NADAC price for package 63561012205

    GET /v1/drugs/nadac/63561012205

Use it

Look up 63561-0122 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63561-0122 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63561-0122. 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.