Micafungin Injection, Powder, Lyophilized, For Solution
FDA Label NDC 70771-1684

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 Micafungin (NDC 70771-1684). 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 70771-1683-6

Micafungin for Injection

50 mg/vial

For Intravenous Infusion Only

10 x 50 mg Single-Dose Vials

Rx only

50 mg Per Vial Carton (4a44243c B3ef 4372 8084 914b28e38d84 01)

50 mg Per Vial Carton (4a44243c B3ef 4372 8084 914b28e38d84 01)

NDC 70771-1684-6

Micafungin for Injection

100 mg/vial

For Intravenous Infusion Only

10 x 100 mg Single-Dose Vials

Rx only

100 mg Per Vial Carton (4a44243c B3ef 4372 8084 914b28e38d84 02)

100 mg Per Vial Carton (4a44243c B3ef 4372 8084 914b28e38d84 02)

* Please review the disclaimer below.