Home NDC 70518-4184-01 NDC 70518-4184-01 - Acetaminophen 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 70518-4184
Requested NDC 70518-4184-01
Package NDCs from labels 70518-4184-1, 70518-4184-0, 70518-4184-3, 70518-4184-2, 70518-4184-01
Manufacturer REMEDYREPACK INC.
Effective date 2026-08-28
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Labels# Label, Manufacturer, Effective date table Label Manufacturer Effective date Type Acetaminophen - REMEDYREPACK INC. REMEDYREPACK INC. 2026-08-28 HUMAN PRESCRIPTION DRUG LABEL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 70518-4184-0 Acetaminophen 24 in 1 CARTON INJECTION, SOLUTION 24 3 70518-4184-1 Acetaminophen 100 mL in 1 VIAL, SINGLE-DOSE INJECTION, SOLUTION 100 3 70518-4184-2 Acetaminophen 25 in 1 CARTON INJECTION, SOLUTION 25 3 70518-4184-3 Acetaminophen 100 mL in 1 VIAL, SINGLE-DOSE INJECTION, SOLUTION 100 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 70518-4184 ACETAMINOPHEN INJECTION, SOLUTION [REMEDYREPACK INC.] 2 Current NDC, 4 package rows 20241003_464e404a-1957-44a2-a53a-f2a9d3c15bde.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 60 of 166 · 3,316 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.