Montelukast Sodium
NDC 67296-1926, Montelukast Sodium, tablet, film coated, from Redpharm Drug.
- Product NDC
- 67296-1926
- Status
- Listed
- Labeler
- Redpharm Drug
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA202717
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/67296-1926 \ -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 |
|---|---|---|
| 67296-1926-3 | 67296192603 | 30 TABLET, FILM COATED in 1 BOTTLE (67296-1926-3) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/2fbdf1be-a37f-879b-e063-6394a90aa20d
Use it
Look up 67296-1926 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/67296-1926 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 67296-1926. 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.