United States · FDA National Drug Code directory
Alendronate Sodium
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0115-1681_0bb7b70c-72e0-4bb8-9d3a-0fc8e4762dd1
- Product NDC
- 0115-1681
- Form
- TABLET
- Composition / generic term
- Alendronate Sodium
- Labeler
- Amneal Pharmaceuticals of New York LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20080206
- Source listing expiry
- 20261231
Source-listed ingredients
- ALENDRONATE SODIUM — 70 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 12 BLISTER PACK in 1 CARTON (0115-1681-26) / 1 TABLET in 1 BLISTER PACK (0115-1681-30) · 0115-1681-26
- 4 BLISTER PACK in 1 CARTON (0115-1681-34) / 1 TABLET in 1 BLISTER PACK (0115-1681-30) · 0115-1681-34
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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