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NDC 78206-172, montelukast sodium, tablet, film coated, from Organon LLC.

Product NDC
78206-172
Status
Listed
Labeler
Organon LLC
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA020829
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/78206-172 \
  -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
78206-172-017820601720130 TABLET, FILM COATED in 1 BOTTLE (78206-172-01)
78206-172-027820601720290 TABLET, FILM COATED in 1 BOTTLE (78206-172-02)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/482dcc92-b47f-4ea6-854a-f5ac2aea7842

  • NADAC price for package 78206017201

    GET /v1/drugs/nadac/78206017201

  • NADAC price for package 78206017202

    GET /v1/drugs/nadac/78206017202

Use it

Look up 78206-172 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/78206-172 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 78206-172. 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.