United States · FDA National Drug Code directory
Zoledronic Acid
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
- 69367-190_ae589b16-5f97-4550-bfc4-5ccf316336fd
- Product NDC
- 69367-190
- Form
- INJECTION
- Composition / generic term
- Zoledronic Acid
- Labeler
- Westminster Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230202 / 20261201
Source-listed ingredients
- ZOLEDRONIC ACID — 4 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL in 1 CARTON (69367-190-50) / 5 mL in 1 VIAL · 69367-190-50
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 →