Package Label.Principal Display Panel
Ibuprofen and famotidine tablets, 800 mg/26.6 mg
90 Tablets
NDC 70771-1924-9
Rx only
Image (099f42a7 F7c9 49f0 8b83 74670cc8124a 01)
Ibuprofen And Famotidine Tablet
FDA Label NDC 70771-1924
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 Ibuprofen And Famotidine (NDC 70771-1924). 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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