Losartan Potassium Tablet, Film Coated
FDA Label NDC 65841-729

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 Losartan Potassium (NDC 65841-729). 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 65841-729-01

Losartan Potassium Tablets USP, 25 mg

Rx Only

100 Tablets

Zydus

Losapotataba (628ca159 4668 4f76 9c62 B541e59416ae 06)

Losapotataba (628ca159 4668 4f76 9c62 B541e59416ae 06)

NDC 65841-730-01

Losartan Potassium Tablets USP, 50 mg

Rx Only

100 Tablets

Zydus

Losapotatabb (628ca159 4668 4f76 9c62 B541e59416ae 07)

Losapotatabb (628ca159 4668 4f76 9c62 B541e59416ae 07)

NDC 65841-731-01

Losartan Potassium Tablets USP, 100 mg

Rx Only

100 Tablets

Zydus

Losapotatabc (628ca159 4668 4f76 9c62 B541e59416ae 08)

Losapotatabc (628ca159 4668 4f76 9c62 B541e59416ae 08)

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