Hexatrione Injection, Suspension
FDA Label NDC 59137-570
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Medexus Pharma, Inc. for the product Hexatrione (NDC 59137-570). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding health care provider letter, how supplied, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
How Supplied
NDC 59137-570-01
- 2 mL single-dose ampoule (40 mg/2mL). One ampoule per carton.
Package Label.Principal Display Panel
20 mg/mL (2 mL Ampoule) - Ampoule Label
20 mg/mL (2 mL Ampoule) - Carton Label
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