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Montelukast Sodium

NDC 71205-778, Montelukast Sodium, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-778
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202468
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-778 \
  -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
71205-778-307120507783030 TABLET, FILM COATED in 1 BOTTLE (71205-778-30)
71205-778-607120507786060 TABLET, FILM COATED in 1 BOTTLE (71205-778-60)
71205-778-907120507789090 TABLET, FILM COATED in 1 BOTTLE (71205-778-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/461f2aaa-e091-478e-97c1-27a089db8cdc

Use it

Look up 71205-778 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-778 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-778. 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.