Alendronate Sodium 16714-0631
Product NDC
16714-0631- Manufacturer
- Northstar Rx Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 4, 2008
- Listing Expires
- December 31, 2027
- Application
- ANDA090124
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Alendronate Sodium | 10 mg/1 |
Drug Class
Bisphosphonate [EPC]Diphosphonates [CS]
Packaging Options(3)
30 TABLET in 1 BOTTLE (16714-631-01)
100 TABLET in 1 BOTTLE (16714-631-02)
10 BLISTER PACK in 1 CARTON (16714-631-11) / 10 TABLET in 1 BLISTER PACK (16714-631-10)