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PREDNISONE

NDC 67046-1610, PREDNISONE, tablet, from Coupler LLC.

Product NDC
67046-1610
Status
Listed
Labeler
Coupler LLC
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/67046-1610 \
  -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
67046-1610-36704616100330 TABLET in 1 BLISTER PACK (67046-1610-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/41e6f1c3-d225-0ff0-e063-6394a90ace88

Use it

Look up 67046-1610 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67046-1610 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67046-1610. 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.