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Mifepristone

NDC 76346-654, Mifepristone, tablet, from Corcept Therapeutics Incorporated.

Product NDC
76346-654
Status
Listed
Labeler
Corcept Therapeutics Incorporated
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA202107
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/76346-654 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MIFEPRISTONE300 mg/1

Pharmacologic classes

Progestational Hormone Receptor Antagonists [MoA]; Progestin Antagonist [EPC]

Package NDCNDC-11Package
76346-654-0376346065403280 TABLET in 1 BOTTLE (76346-654-03)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/63c068cd-9370-460f-829b-70e8c7ebe91e

Use it

Look up 76346-654 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76346-654 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76346-654. 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.