Montelukast Sodium 68788-8617
Product NDC
68788-8617- Manufacturer
- Preferred Pharmaceuticals Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 28, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA204290
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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(3)
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8617-3)
60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8617-6)
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-8617-9)