Home NDC 72189-426 NDC 72189-426 - Oxycodone/APAP 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 72189-426
Package NDCs from labels 72189-426-30, 72189-426-60, 72189-426-90, 72189-426-72
Manufacturer Direct_Rx
Effective date 2023-07-24
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Oxycodone/APAP - Direct_Rx Direct_Rx 2023-07-24 HUMAN PRESCRIPTION DRUG LABEL
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 72189-426-30 Oxycodone/APAP 30 in 1 BOTTLE TABLET 30 4 72189-426-60 Oxycodone/APAP 60 in 1 BOTTLE TABLET 60 4 72189-426-72 Oxycodone/APAP 120 in 1 BOTTLE TABLET 120 4 72189-426-90 Oxycodone/APAP 90 in 1 BOTTLE TABLET 90 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 72189-426 OXYCODONE/APAP TABLET [DIRECT_RX] 4 4 package rows 20230725_f53bfa4e-e4a4-cfb6-e053-2995a90a7ba1.zip