Ibuprofen Tablet, Film Coated
FDA Label NDC 71335-1503

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Bryant Ranch Prepack for the product Ibuprofen (NDC 71335-1503). 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

How Supplied

Product: 71335-1396

NDC: 71335-1396-0 84 TABLET, FILM COATED in a BOTTLE

NDC: 71335-1396-1 20 TABLET, FILM COATED in a BOTTLE

NDC: 71335-1396-2 15 TABLET, FILM COATED in a BOTTLE

NDC: 71335-1396-3 40 TABLET, FILM COATED in a BOTTLE

NDC: 71335-1396-4 21 TABLET, FILM COATED in a BOTTLE

NDC: 71335-1396-5 30 TABLET, FILM COATED in a BOTTLE

NDC: 71335-1396-6 90 TABLET, FILM COATED in a BOTTLE

NDC: 71335-1396-7 100 TABLET, FILM COATED in a BOTTLE

NDC: 71335-1396-8 120 TABLET, FILM COATED in a BOTTLE

NDC: 71335-1396-9 60 TABLET, FILM COATED in a BOTTLE

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