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PREDNISOLONE

NDC 59651-491, PREDNISOLONE, tablet, from Aurobindo Pharma Limited.

Product NDC
59651-491
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215673
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-491 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PREDNISOLONE5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
59651-491-0159651049101100 TABLET in 1 BOTTLE (59651-491-01)
59651-491-505965104915050 TABLET in 1 BOTTLE (59651-491-50)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/070f1937-50a5-457f-bef5-4e597014e26d

  • NADAC price for package 59651049101

    GET /v1/drugs/nadac/59651049101

Use it

Look up 59651-491 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-491 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-491. 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.