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Prednisone

NDC 76420-069, Prednisone, tablet, from Asclemed USA, Inc..

Product NDC
76420-069
Status
Listed
Labeler
Asclemed USA, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA040362
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76420-069 \
  -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
76420-069-107642000691010 TABLET in 1 BOTTLE (76420-069-10)
76420-069-157642000691515 TABLET in 1 BOTTLE (76420-069-15)
76420-069-207642000692020 TABLET in 1 BOTTLE (76420-069-20)
76420-069-217642000692121 TABLET in 1 BOTTLE (76420-069-21)
76420-069-307642000693030 TABLET in 1 BOTTLE (76420-069-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dc663fd3-b149-48ae-a3f3-6abaa4808cc6

Use it

Look up 76420-069 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-069 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-069. 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.