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prednisone

NDC 42708-166, PREDNISONE, tablet, from QPharma Inc.

Product NDC
42708-166
Status
Listed
Labeler
QPharma Inc
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA208412
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/42708-166 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PREDNISONE10 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
42708-166-214270801662121 TABLET in 1 BOTTLE, PLASTIC (42708-166-21)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f795ea1d-f41a-6100-e053-6394a90a63a4

Use it

Look up 42708-166 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42708-166 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42708-166. 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.