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Montelukast

NDC 50268-556, Montelukast, tablet, film coated, from AvPAK.

Product NDC
50268-556
Status
Listed
Labeler
AvPAK
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/50268-556 \
  -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
50268-556-155026805561550 BLISTER PACK in 1 BOX (50268-556-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-556-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/d7870c45-5a8b-8369-e053-2a95a90ae1f3

  • NADAC price for package 50268055615

    GET /v1/drugs/nadac/50268055615

Use it

Look up 50268-556 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50268-556 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50268-556. 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.