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Exemestane

NDC 51991-005, Exemestane, tablet, film coated, from Breckenridge Pharmaceutical, Inc..

Product NDC
51991-005
Status
Listed
Labeler
Breckenridge Pharmaceutical, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211031
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51991-005 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • EXEMESTANE25 mg/1

Pharmacologic classes

Aromatase Inhibitor [EPC]; Aromatase Inhibitors [MoA]

Package NDCNDC-11Package
51991-005-905199100059090 TABLET, FILM COATED in 1 BOTTLE (51991-005-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4e3fd382-19f5-4ded-ab22-39d5b1b2f366

  • NADAC price for package 51991000590

    GET /v1/drugs/nadac/51991000590

Use it

Look up 51991-005 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51991-005 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51991-005. 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.