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
- 0054-0282_56e063a8-8c3d-4445-91fd-0c8806c2b127
- Product NDC
- 0054-0282
- Form
- SOLUTION
- Composition / generic term
- Alendronate Sodium
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20201030
- Source listing expiry
- 20271231
Source-listed ingredients
- ALENDRONATE SODIUM — 70 mg/75mL
These values do not establish equivalence or a dose recommendation.
Packages
- 4 BOTTLE, UNIT-DOSE in 1 CARTON (0054-0282-59) / 75 mL in 1 BOTTLE, UNIT-DOSE · 0054-0282-59
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →