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PredniSONE

NDC 51655-939, PredniSONE, tablet, from Northwind Health Company, LLC.

Product NDC
51655-939
Status
Listed
Labeler
Northwind Health Company, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA084283
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51655-939 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PREDNISONE50 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
51655-939-07516550939077 TABLET in 1 BOTTLE, PLASTIC (51655-939-07)
51655-939-55516550939555 TABLET in 1 BOTTLE, PLASTIC (51655-939-55)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f77f4a5a-b307-84ff-e053-6294a90aba5b

Use it

Look up 51655-939 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-939 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-939. 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.