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
- 68071-3340_54f0bd6e-614e-f240-e063-6394a90a2a25
- Product NDC
- 68071-3340
- Form
- TABLET
- Composition / generic term
- Alendronate sodium
- Labeler
- NuCare Pharmaceuticals,Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20080804
- Source listing expiry
- 20271231
Source-listed ingredients
- ALENDRONATE SODIUM — 70 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 4 TABLET in 1 BOX (68071-3340-4) · 68071-3340-4
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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