Ibuprofen Tablet, Film Coated
FDA Label NDC 51655-474

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Northwind Health Company, Llc for the product Ibuprofen (NDC 51655-474). 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 ibuprofen tablets 400 mg - 600 mg- 800 mg medguide, how supplied, 600 mg 30 count label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

How Supplied

600mg (white to off white, capsule shaped, biconvex, film coated tablets debossed with '122' on one side and plain on the other side) Bottles of 20 NDC: 51655-474-20, 30 NDC: 51655-474-52, 40 NDC: 51655-474-51, 60 NDC: 51655-474-25, and 90 NDC: 51655-474-90.

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