NDC 65862-329 – Alendronate Sodium
Alendronate Sodium 70 mg/1 · Tablet · Oral
Product NDC65862-329
Product details
- Brand name
- Alendronate Sodium
- Generic name
- Alendronate Sodium
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA090124
- Marketed since
- August 4, 2008
- Listing expires
- December 31, 2027
- Pharmacologic class
- Bisphosphonate
Active ingredients
- Alendronate Sodium 70 mg/1
Uses, dosage, side effects and warnings for Alendronate Sodium →
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 65862-329-01 | 100 TABLET in 1 BOTTLE (65862-329-01) | Mar 6, 2024 |
| 65862-329-04 | 1 BLISTER PACK in 1 CARTON (65862-329-04) / 4 TABLET in 1 BLISTER PACK | Aug 4, 2008 |
| 65862-329-05 | 500 TABLET in 1 BOTTLE (65862-329-05) | Mar 6, 2024 |
| 65862-329-08 | 3 BLISTER PACK in 1 CARTON (65862-329-08) / 4 TABLET in 1 BLISTER PACK | Aug 4, 2008 |
| 65862-329-10 | 10 BLISTER PACK in 1 CARTON (65862-329-10) / 10 TABLET in 1 BLISTER PACK | Aug 4, 2008 |
| 65862-329-20 | 5 BLISTER PACK in 1 CARTON (65862-329-20) / 4 TABLET in 1 BLISTER PACK | Aug 4, 2008 |
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