Montelukast 68001-0361
Product NDC
68001-0361- Manufacturer
- Bluepoint Laboratories
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- June 29, 2018
- Listing Expires
- December 31, 2026
- Application
- ANDA203366
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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)
500 TABLET in 1 BOTTLE (68001-361-03)
30 TABLET in 1 BOTTLE (68001-361-04)
90 TABLET in 1 BOTTLE (68001-361-05)