Ibuprofen Tablet, Film Coated
FDA Label NDC 68071-3362

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Nucare Pharmaceuticals,inc. for the product Ibuprofen (NDC 68071-3362). 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 how supplied, 800mg ibuprofen package label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

How Supplied

NDC 68071-3362-0 Bottles of 12

NDC 68071-3362-5 Bottles of 15

NDC 68071-3362-2 Bottles of 20

NDC 68071-3362-2 Bottles of 21

NDC 68071-3362-3 Bottles of 30

NDC 68071-3362-4 Bottles of 40

NDC 68071-3362-6 Bottles of 60

NDC 68071-3362-9 Bottles of 90

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