Home NDC 80425-0132-01 NDC 80425-0132-01 - Ibuprofen This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 80425-0132
Requested NDC 80425-0132-01
Package NDCs from labels 80425-0132-3, 80425-0132-2, 80425-0132-1, 80425-0132-01
Manufacturer Advanced Rx Pharmacy of Tennessee, LLC | Advanced Rx Pharmacy of Tennseess, LLC
Effective date 2024-12-31
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Ibuprofen Tablets Advanced Rx Pharmacy of Tennessee, LLC | Advanced Rx Pharmacy of Tennseess, LLC 2024-12-31 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 80425-0132-1 Ibuprofen 30 in 1 BOTTLE TABLET, FILM COATED 30 7 80425-0132-2 Ibuprofen 60 in 1 BOTTLE TABLET, FILM COATED 60 7 80425-0132-3 Ibuprofen 90 in 1 BOTTLE TABLET, FILM COATED 90 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 80425-0132 IBUPROFEN TABLET, FILM COATED [ADVANCED RX PHARMACY OF TENNESSEE, LLC] 7 Current NDC, Legacy NDC, 3 package rows 20250101_bd1ca7af-d640-23fb-e053-2a95a90a8a98.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 18 of 57 · 1,124 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.