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Prednisone

NDC 42708-105, Prednisone, tablet, from QPharma, Inc..

Product NDC
42708-105
Status
Listed
Labeler
QPharma, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA085161
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42708-105 \
  -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
42708-105-104270801051010 TABLET in 1 BOTTLE (42708-105-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d898d53f-c7d2-4bdb-bd9e-5f200070d123

Use it

Look up 42708-105 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42708-105 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42708-105. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.