Hydrocortisone Sodium Succinate Injection
FDA Label NDC 70771-1966

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Zydus Lifesciences Limited for the product Hydrocortisone Sodium Succinate (NDC 70771-1966). 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 package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Package Label.Principal Display Panel

NDC 70771-1966-1

Hydrocortisone sodium succinate for injection, USP

100 mg/vial

For Intravenous or Intramuscular use

Rx only

Vial Label (23cd0282 Fb6b 4fb9 9b3a 0b23e8125625 01)

Vial Label (23cd0282 Fb6b 4fb9 9b3a 0b23e8125625 01)

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