United States · FDA National Drug Code directory
IBANDRONATE 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
- 69452-378_55845f3d-9d8b-4426-96ea-e73438e380d1
- Product NDC
- 69452-378
- Form
- TABLET
- Composition / generic term
- IBANDRONATE SODIUM
- Labeler
- Bionpharma Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230526
- Source listing expiry
- 20271231
Source-listed ingredients
- IBANDRONATE SODIUM — 150 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (69452-378-74) / 3 TABLET in 1 BLISTER PACK · 69452-378-74
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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