Alendronate Sodium 68071-3771
Product NDC
68071-3771- Manufacturer
- Nucare Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 4, 2008
- Listing Expires
- December 31, 2026
- Application
- ANDA076768
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Alendronate Sodium | 70 mg/1 |
Drug Class
Bisphosphonate [EPC]Diphosphonates [CS]
Packaging Options(1)
15 BLISTER PACK in 1 CARTON (68071-3771-5) / 1 TABLET in 1 BLISTER PACK