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
- 76282-681_2012c7a8-8aa7-4c18-a8c3-fe74d74ac873
- Product NDC
- 76282-681
- Form
- TABLET
- Composition / generic term
- Alendronate sodium
- Labeler
- EXELAN PHARMACEUTICALS INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210202
- Source listing expiry
- 20261231
Source-listed ingredients
- ALENDRONATE SODIUM — 35 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 BLISTER PACK in 1 CARTON (76282-681-46) / 4 TABLET in 1 BLISTER PACK (76282-681-45) · 76282-681-46
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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