NDC 69097-223 – Alendronate Sodium
Alendronate Sodium 35 mg/1 · Tablet · Oral
Product NDC69097-223
Product details
- Brand name
- Alendronate Sodium
- Generic name
- Alendronate sodium
- Labeler
- Cipla USA Inc.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076768
- Marketed since
- August 4, 2008
- Listing expires
- December 31, 2027
- 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 |
|---|---|---|
| 69097-223-16 | 1 BLISTER PACK in 1 CARTON (69097-223-16) / 4 TABLET in 1 BLISTER PACK | Aug 4, 2008 |
| 69097-223-76 | 3 BLISTER PACK in 1 CARTON (69097-223-76) / 4 TABLET in 1 BLISTER PACK | Aug 4, 2008 |
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