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
- 62756-079_55b2d0db-98cd-036e-e063-6394a90ab69c
- Product NDC
- 62756-079
- Form
- INJECTION, SOLUTION
- Composition / generic term
- sugammadex
- Labeler
- Sun Pharmaceutical Industries, 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 (62756-079-02) / 2 mL in 1 VIAL, SINGLE-DOSE (62756-079-01) · 62756-079-02
- 10 VIAL, SINGLE-DOSE in 1 CARTON (62756-079-04) / 5 mL in 1 VIAL, SINGLE-DOSE (62756-079-03) · 62756-079-04
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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