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Montelukast

NDC 68788-8099, Montelukast, tablet, film coated, from Preferred Pharmaceuticals, Inc..

Product NDC
68788-8099
Status
Listed
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202843
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8099 \
  -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
68788-8099-36878880990330 TABLET, FILM COATED in 1 BOTTLE (68788-8099-3)
68788-8099-66878880990660 TABLET, FILM COATED in 1 BOTTLE (68788-8099-6)
68788-8099-96878880990990 TABLET, FILM COATED in 1 BOTTLE (68788-8099-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/94642db1-5c75-44c4-92b4-8385b486df82

Use it

Look up 68788-8099 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8099 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-8099. 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.