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Exemestane

NDC 71921-190, Exemestane, tablet, film coated, from Florida Pharmaceutical Products, LLC.

Product NDC
71921-190
Status
Listed
Labeler
Florida Pharmaceutical Products, LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213547
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71921-190 \
  -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
71921-190-337192101903330 TABLET, FILM COATED in 1 BOTTLE (71921-190-33)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/9354d1a1-8e8c-4c6a-b7ad-d4fe14b10a8b

  • NADAC price for package 71921019033

    GET /v1/drugs/nadac/71921019033

Use it

Look up 71921-190 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71921-190 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71921-190. 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.