NDC 0115-1679 – Alendronate Sodium
Alendronate Sodium 35 mg/1 · Tablet · Oral
Product NDC0115-1679
Product details
- Brand name
- Alendronate Sodium
- Generic name
- Alendronate Sodium
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA075710
- Marketed since
- February 6, 2008
- Listing expires
- December 31, 2026
- Pharmacologic class
- Bisphosphonate
Active ingredients
- Alendronate Sodium 35 mg/1
Uses, dosage, side effects and warnings for Alendronate Sodium →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0115-1679-26 | 12 BLISTER PACK in 1 CARTON (0115-1679-26) / 1 TABLET in 1 BLISTER PACK (0115-1679-30) | Feb 6, 2008 |
| 0115-1679-34 | 4 BLISTER PACK in 1 CARTON (0115-1679-34) / 1 TABLET in 1 BLISTER PACK (0115-1679-30) | Feb 6, 2008 |
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