United States · FDA National Drug Code directory
gadobutrol
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
- 70710-2064_4bdf7135-c236-4892-96e0-db2d78d53853
- Product NDC
- 70710-2064
- Form
- INJECTION
- Composition / generic term
- gadobutrol
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260714
- Source listing expiry
- 20271231
Source-listed ingredients
- GADOBUTROL — 604.72 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL, SINGLE-DOSE in 1 CARTON (70710-2064-6) / 7.5 mL in 1 VIAL, SINGLE-DOSE (70710-2064-1) · 70710-2064-6
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 →