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montelukast sodium

NDC 71205-181, montelukast sodium, tablet, film coated, from Proficient Rx LP.

Product NDC
71205-181
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA204290
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-181 \
  -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
71205-181-307120501813030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-181-30)
71205-181-607120501816060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-181-60)
71205-181-907120501819090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-181-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2ce48faf-4504-488a-8b20-3e8d4f008fb2

Use it

Look up 71205-181 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-181 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-181. 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.