Home NDC 80425-0348-01 NDC 80425-0348-01 - Dyural 40 Kit 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 80425-0348
Requested NDC 80425-0348-01
Package NDCs from labels 80425-0348-1, 80425-0348-01
Manufacturer Advanced Rx Pharmacy 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 0409-4887-17 Dyural 40 Kit 10 mL in 1 VIAL, PLASTIC INJECTION 10 mL 1 mL in 1mL 2 0409-4888-02 Dyural 40 Kit 10 mL in 1 VIAL, SINGLE-DOSE INJECTION, SOLUTION 10 mL 9 mg in 1mL 2 70121-1573-5 Dyural 40 Kit 25 in 1 CARTON INJECTION, SUSPENSION 40 mg in 1mL 2 70121-1573-5 Dyural 40 Kit 1 mL in 1 VIAL, SINGLE-DOSE INJECTION, SUSPENSION 1 mL 40 mg in 1mL 2 80425-0348-1 Dyural 40 Kit 1 in 1 CARTON KIT 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 80425-0348 DYURAL 40 KIT (METHYLPREDNISOLONE ACETATE, LIDOCAINE HYDROCHLORIDE, BUPIVACAINE HYDROCHLORIDE, POVIDINE IODINE, SODIUM CHLORIDE, ISOPROPYL ALCOHOL) KIT [ADVANCED RX PHARMACY OF TENNESSEE, LLC] 2 Current NDC, 5 package rows 20250102_01ca16de-ab2e-4e19-e063-6394a90a0510.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 89 of 239 · 4,780 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.