How Supplied
Product: 53002-3372
NDC: 53002-3372-1 15 TABLET, FILM COATED in a BOTTLE
NDC: 53002-3372-3 30 TABLET, FILM COATED in a BOTTLE
NDC: 53002-3372-5 50 TABLET, FILM COATED in a BOTTLE
Ibuprofen
FDA Label NDC 53002-3372
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Rpk Pharmaceuticals, Inc. for the product Ibuprofen (NDC 53002-3372). 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, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
* Please review the disclaimer below.
