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Letrozole

NDC 17856-0032, letrozole, tablet, film coated, from ATLANTIC BIOLOGICALS CORP..

Product NDC
17856-0032
Status
Listed
Labeler
ATLANTIC BIOLOGICALS CORP.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090934
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/17856-0032 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LETROZOLE2.5 mg/1

Pharmacologic classes

Aromatase Inhibitor [EPC]; Aromatase Inhibitors [MoA]

Package NDCNDC-11Package
17856-0032-117856003201100 POUCH in 1 BOX, UNIT-DOSE (17856-0032-1) / 1 TABLET, FILM COATED in 1 POUCH

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c10bf97f-f9cf-468a-8a1f-7637f41022e4

Use it

Look up 17856-0032 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/17856-0032 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 17856-0032. 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.