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Montelukast

NDC 72865-175, Montelukast, tablet, film coated, from XLCare Pharmaceuticals Inc..

Product NDC
72865-175
Status
Listed
Labeler
XLCare Pharmaceuticals Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202843
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72865-175 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • MONTELUKAST SODIUM10 mg/1

Pharmacologic classes

Leukotriene Receptor Antagonist [EPC]; Leukotriene Receptor Antagonists [MoA]

Package NDCNDC-11Package
72865-175-10728650175101000 TABLET, FILM COATED in 1 BOTTLE (72865-175-10)
72865-175-307286501753030 TABLET, FILM COATED in 1 BOTTLE (72865-175-30)
72865-175-907286501759090 TABLET, FILM COATED in 1 BOTTLE (72865-175-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/82d65eea-c7c9-4e16-9176-46c43f00f0f6

Use it

Look up 72865-175 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72865-175 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72865-175. 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.