NDC 76282-681 – Alendronate Sodium
Alendronate Sodium 35 mg/1 · Tablet · Oral
Product NDC76282-681
Product details
- Brand name
- Alendronate Sodium
- Generic name
- Alendronate sodium
- Labeler
- EXELAN PHARMACEUTICALS INC.
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076768
- Marketed since
- February 2, 2021
- 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 (1)
| Package NDC | Description | Since |
|---|---|---|
| 76282-681-46 | 3 BLISTER PACK in 1 CARTON (76282-681-46) / 4 TABLET in 1 BLISTER PACK (76282-681-45) | Feb 2, 2021 |
Other Alendronate Sodium products
- 50090-3126 Alendronate Sodium 70 mg/1 · Tablet · A-S Medication Solutions
- 50090-4692 Alendronate Sodium 70 mg/1 · Tablet · A-S Medication Solutions
- 50090-5474 Alendronate Sodium 35 mg/1 · Tablet · A-S Medication Solutions
- 50090-5677 Alendronate Sodium 70 mg/1 · Tablet · A-S Medication Solutions
- 0115-1676 Alendronate Sodium 5 mg/1 · Tablet · Amneal Pharmaceuticals of New York LLC
- 0115-1678 Alendronate Sodium 10 mg/1 · Tablet · Amneal Pharmaceuticals of New York LLC
- 0115-1679 Alendronate Sodium 35 mg/1 · Tablet · Amneal Pharmaceuticals of New York LLC
- 0115-1680 Alendronate Sodium 40 mg/1 · Tablet · Amneal Pharmaceuticals of New York LLC
- 0115-1681 Alendronate Sodium 70 mg/1 · Tablet · Amneal Pharmaceuticals of New York LLC
- 65862-327 Alendronate Sodium 10 mg/1 · Tablet · Aurobindo Pharma Limited
- 65862-329 Alendronate Sodium 70 mg/1 · Tablet · Aurobindo Pharma Limited
- 65862-328 Alendronate Sodium 35 mg/1 · Tablet · Aurobindo Pharma Limited