Montelukast Sodium 00904-6808
Product NDC
00904-6808- Manufacturer
- Major Pharmaceuticals
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 10, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA202843
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Montelukast Sodium | 10 mg/1 |
Drug Class
Leukotriene Receptor Antagonist [EPC]Leukotriene Receptor Antagonists [MoA]
Packaging Options(2)
50 BLISTER PACK in 1 CARTON (0904-6808-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK
100 BLISTER PACK in 1 CARTON (0904-6808-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK