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PredniSONE Tablets, USP, 20 mg

NDC 71335-2938, PredniSONE, tablet, from Bryant Ranch Prepack.

Product NDC
71335-2938
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212629
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2938 \
  -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
71335-2938-1713352938019 TABLET in 1 BOTTLE (71335-2938-1)
71335-2938-27133529380219 TABLET in 1 BOTTLE (71335-2938-2)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/852ea185-1bda-4c89-a192-ee0f93cba428

Use it

Look up 71335-2938 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-2938 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-2938. 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.