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PREDNISONE

NDC 59651-485, PREDNISONE, tablet, from Aurobindo Pharma Limited.

Product NDC
59651-485
Status
Listed
Labeler
Aurobindo Pharma Limited
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215672
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/59651-485 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PREDNISONE2.5 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
59651-485-0159651048501100 TABLET in 1 BOTTLE (59651-485-01)
59651-485-785965104857810 BLISTER PACK in 1 CARTON (59651-485-78) / 10 TABLET in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b1ac4c92-e1fd-4015-b172-0932790ae019

  • NADAC price for package 59651048501

    GET /v1/drugs/nadac/59651048501

Use it

Look up 59651-485 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/59651-485 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 59651-485. 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.