Package Label.Principal Display Panel
NDC 70771-1520-8
Sevelamer Tablets, 800 mg
270 Tablets
Rx only
Label (B2409df0 E9ba 42fc Ba50 A45d5e7e36d6 01)
Sevelamer Carbonate Tablet, Film Coated
FDA Label NDC 70771-1520
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 Sevelamer Carbonate (NDC 70771-1520). 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.
Label Section Quick Index
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