Home NDC 70518-2358-01 NDC 70518-2358-01 - Diazepam 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 70518-2358
Requested NDC 70518-2358-01
Package NDCs from labels 70518-2358-0, 70518-2358-2, 70518-2358-1, 70518-2358-01
Manufacturer REMEDYREPACK INC.
Effective date 2026-10-06
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type DIAZEPAM INJECTION, USP REMEDYREPACK INC. 2026-10-06 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70518-2358-0 Diazepam 10 in 1 CARTON INJECTION, SOLUTION 10 17 70518-2358-0 Diazepam 2 mL in 1 SYRINGE, GLASS INJECTION, SOLUTION 2 17 70518-2358-1 Diazepam 10 in 1 CARTON INJECTION, SOLUTION 10 17 70518-2358-2 Diazepam 2 mL in 1 SYRINGE, GLASS INJECTION, SOLUTION 2 17
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70518-2358 DIAZEPAM INJECTION, SOLUTION [REMEDYREPACK INC.] 11 Current NDC, Legacy NDC, 4 package rows 20250426_c57af2a2-aa9a-4dac-a200-e0d845005d05.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 6 of 155 · 3,089 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.