NDC 68462-695 – Sugammadex

Sugammadex Sodium 200 mg/2mL · Injection, Solution · Intravenous

Human Prescription Drug

Product NDC68462-695

Product details

Brand name
Sugammadex
Generic name
Sugammadex
Labeler
GLENMARK PHARMACEUTICALS INC., USA
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA214364
Marketed since
July 28, 2026
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Sugammadex →

Package NDC codes (1)

Package NDCDescriptionSince
68462-695-2010 VIAL, SINGLE-DOSE in 1 CARTON (68462-695-20) / 2 mL in 1 VIAL, SINGLE-DOSE (68462-695-02)Jul 28, 2026

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