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Mifepristone

NDC 43393-001, MIFEPRISTONE, tablet, from GenBioPro, Inc..

Product NDC
43393-001
Status
Listed
Labeler
GenBioPro, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA091178
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/43393-001 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MIFEPRISTONE200 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
43393-001-06433930001066 CARTON in 1 PACKAGE (43393-001-06) / 1 BLISTER PACK in 1 CARTON / 1 TABLET in 1 BLISTER PACK (43393-001-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b63fad9b-7f12-4400-9019-b0586054e534

Use it

Look up 43393-001 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/43393-001 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 43393-001. 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.