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
- 70748-371_a848d653-aec4-46d5-82dc-80c0aa6d249c
- Product NDC
- 70748-371
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Sugammadex
- Labeler
- Lupin Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260728
- Source listing expiry
- 20271231
Source-listed ingredients
- SUGAMMADEX SODIUM — 100 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 VIAL, SINGLE-DOSE in 1 CARTON (70748-371-02) / 5 mL in 1 VIAL, SINGLE-DOSE (70748-371-01) · 70748-371-02
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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