Montelukast
NDC 82009-009, Montelukast, tablet, film coated, from Quallent Pharmaceuticals Health LLC.
- Product NDC
- 82009-009
- Status
- Listed
- Labeler
- Quallent Pharmaceuticals Health LLC
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA202843
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/82009-009 \ -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 NDC | NDC-11 | Package |
|---|---|---|
| 82009-009-10 | 82009000910 | 1000 TABLET, FILM COATED in 1 BOTTLE (82009-009-10) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/5d71088b-b0fa-4bf0-a6e7-6163bd9e0dd4NADAC price for package 82009000910
GET /v1/drugs/nadac/82009000910
Use it
Look up 82009-009 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/82009-009 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 82009-009. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.