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Montelukast

NDC 0781-5560, Montelukast, tablet, film coated, from Sandoz Inc.

Product NDC
0781-5560
Status
Listed
Labeler
Sandoz Inc
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA200889
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0781-5560 \
  -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
0781-5560-130078155601310 BLISTER PACK in 1 CARTON (0781-5560-13) / 10 TABLET, FILM COATED in 1 BLISTER PACK (0781-5560-06)
0781-5560-310078155603130 TABLET, FILM COATED in 1 BOTTLE (0781-5560-31)
0781-5560-920078155609290 TABLET, FILM COATED in 1 BOTTLE (0781-5560-92)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/6d69e73a-76cb-4ece-9cf9-e9adb4f523b4

Use it

Look up 0781-5560 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0781-5560 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0781-5560. 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.