Trazodone Hydrochloride Tablet
FDA Label NDC 70771-1939

The following Structured Product Label (SPL) was submitted to the FDA by Zydus Lifesciences Limited for the product Trazodone Hydrochloride (NDC 70771-1939). 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 70771-1128-1

Trazodone Hydrochloride Tablets USP, 50 mg

100 Tablets

Rx only

Trazodone Hyadrochloride Tablets, Usp (996a344d B21d 4078 A61e Fb812728e5d3 10)

NDC 70771-1129-1

Trazodone Hydrochloride Tablets USP, 100 mg

100 Tablets

Rx only

Trazodone Hyadrochloride Tablets, Usp (996a344d B21d 4078 A61e Fb812728e5d3 11)

NDC 70771-1130-1

Trazodone Hydrochloride Tablets USP, 150 mg

100 Tablets

Rx only

Trazodone Hyadrochloride Tablets, Usp (996a344d B21d 4078 A61e Fb812728e5d3 12)

NDC 70771-1131-1

Trazodone Hydrochloride Tablets USP, 300 mg

100 Tablets

Rx only

Trazodone Hyadrochloride Tablets, Usp (996a344d B21d 4078 A61e Fb812728e5d3 13)

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