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Montelukast Sodium

NDC 65162-732, Montelukast, tablet, from Amneal Pharmaceuticals LLC.

Product NDC
65162-732
Status
Listed
Labeler
Amneal Pharmaceuticals LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204604
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65162-732 \
  -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
65162-732-036516207320330 TABLET in 1 BOTTLE (65162-732-03)
65162-732-096516207320990 TABLET in 1 BOTTLE (65162-732-09)
65162-732-11651620732111000 TABLET in 1 BOTTLE (65162-732-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ccbbf0d6-efd9-4fdd-9e7b-e3d293062609

Use it

Look up 65162-732 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65162-732 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65162-732. 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.