United States · FDA National Drug Code directory
Sugammadex
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
- 70710-1651_0f34bfb3-63e1-406c-a3c6-654e120e5957
- Product NDC
- 70710-1651
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Sugammadex
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260702
- Source listing expiry
- 20271231
Source-listed ingredients
- SUGAMMADEX SODIUM — 500 mg/5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL, SINGLE-DOSE in 1 CARTON (70710-1651-6) / 5 mL in 1 VIAL, SINGLE-DOSE (70710-1651-1) · 70710-1651-6
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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