Home NDC 80425-0070-01 NDC 80425-0070-01 - Omeprazole DR 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 80425-0070
Requested NDC 80425-0070-01
Package NDCs from labels 80425-0070-4, 80425-0070-2, 80425-0070-1, 80425-0070-3, 80425-0070-01
Manufacturer Advanced Rx of Tennessee, LLC
Effective date 2024-12-31
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 80425-0070-1 OmeprazoleDR 30 in 1 BOTTLE CAPSULE, DELAYED RELEASE 30 10 80425-0070-2 OmeprazoleDR 60 in 1 BOTTLE CAPSULE, DELAYED RELEASE 60 10 80425-0070-3 OmeprazoleDR 120 in 1 BOTTLE CAPSULE, DELAYED RELEASE 120 10 80425-0070-4 OmeprazoleDR 90 in 1 BOTTLE CAPSULE, DELAYED RELEASE 90 10
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 80425-0070 OMEPRAZOLE DR (OMEPRAZOLE) CAPSULE, DELAYED RELEASE [ADVANCED RX OF TENNESSEE, LLC] 10 Current NDC, Legacy NDC, 4 package rows 20250101_af85afda-6b0c-d657-e053-2a95a90afb4b.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 8 of 15 · 291 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.