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
63323-966_9fb5ae91-44b4-4b48-aaeb-0a2ba676aa16
Product NDC
63323-966
Form
INJECTION, SOLUTION
Composition / generic term
Zoledronic Acid
Labeler
Fresenius Kabi USA, LLC
Marketing category
ANDA
Marketing start / end (source format)
20170217
Source listing expiry
20261231

Source-listed ingredients

  • ZOLEDRONIC ACID — 5 mg/100mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL, GLASS in 1 CARTON (63323-966-00) / 100 mL in 1 VIAL, GLASS · 63323-966-00

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 →
Zoledronic Acid — United States | Molindra Medicines